| Device | CLASS II | 100230-10-DEX100, Liquid Concentrate recalled by Diasol | Diasol | Other | Nationwide |
| Device | CLASS II | Affixus Antegrade Femoral Nailing System Affixus Antegrade recalled | Zimmer | Device Malfunction | Nationwide |
| Device | CLASS II | Affixus Antegrade Femoral Nailing System Affixus Antegrade recalled | Zimmer | Device Malfunction | Nationwide |
| Device | CLASS II | Affixus Antegrade Femoral Nailing System Affixus Antegrade recalled | Zimmer | Device Malfunction | Nationwide |
| Device | CLASS I | Vapor 3000. Unheated, calibrated anesthetic vaporizer recalled | Draeger | Potency & Assay | Nationwide |
| Device | CLASS I | Alcon Laboratories, Inc Custom Pak recalled by Alcon Research | Alcon Research | Sterility | Nationwide |
| Device | CLASS II | 100125-10-DEX100, Liquid Concentrate recalled by Diasol | Diasol | Other | Nationwide |
| Device | CLASS II | Ring Transjugular Intrahepatic Access Sets recalled by Cook Incorporated | Cook | Potency & Assay | IN |
| Device | CLASS II | Beckman Coulter Bicarbonate recalled | Beckman Coulter Ireland | Other | Nationwide |
| Device | CLASS II | Affixus Antegrade Femoral Nailing System Affixus Antegrade recalled | Zimmer | Device Malfunction | Nationwide |
| Device | CLASS II | Affixus Antegrade Femoral Nailing System Affixus Antegrade recalled | Zimmer | Device Malfunction | Nationwide |
| Device | CLASS II | Affixus Antegrade Femoral Nailing System Affixus Antegrade recalled | Zimmer | Device Malfunction | Nationwide |
| Device | CLASS II | 100325-10-DEX100, Liquid Concentrate recalled by Diasol | Diasol | Other | Nationwide |
| Device | CLASS II | Affixus Antegrade Femoral Nailing System Affixus Antegrade recalled | Zimmer | Device Malfunction | Nationwide |
| Device | CLASS II | Affixus Antegrade Femoral Nailing System Affixus Antegrade recalled | Zimmer | Device Malfunction | Nationwide |
| Device | CLASS II | R¿sch-Uchida Transjugular Liver Access Sets recalled | Cook | Potency & Assay | IN |
| Device | CLASS II | Lyfo Disk, Campylobacter jejuni subsp recalled by Microbiologics | Microbiologics | Other Bacterial Contamination | Nationwide |
| Device | CLASS II | Kwik-stik, Campylobacter jejuni subsp recalled by Microbiologics | Microbiologics | Other Bacterial Contamination | Nationwide |
| Device | CLASS II | Brand name: Agfa Digital Radiography X- Ray system DR recalled | Agfa Healthcare | Other | Nationwide |
| Device | CLASS II | Affixus Antegrade Femoral Nailing System Affixus Antegrade recalled | Zimmer | Device Malfunction | Nationwide |
| Device | CLASS II | LifeShield Drug Library Management (DLM), LifeShield Infusion Safety recalled | ICU Medical | Device Malfunction | Nationwide |
| Device | CLASS II | Affixus Antegrade Femoral Nailing System Affixus Antegrade recalled | Zimmer | Device Malfunction | Nationwide |
| Device | CLASS II | Affixus Antegrade Femoral Nailing System Affixus Antegrade recalled | Zimmer | Device Malfunction | Nationwide |
| Device | CLASS II | Affixus Antegrade Femoral Nailing System Affixus Antegrade recalled | Zimmer | Device Malfunction | Nationwide |
| Device | CLASS II | Affixus Antegrade Femoral Nailing System Affixus Antegrade recalled | Zimmer | Device Malfunction | Nationwide |
| Device | CLASS II | Affixus Antegrade Femoral Nailing System Affixus Antegrade recalled | Zimmer | Device Malfunction | Nationwide |
| Device | CLASS II | da Vinci 5, Surgeon Console Column Motor Connector recalled | Intuitive Surgical | Other | Nationwide |
| Device | CLASS II | 100220-10-DEX100, Liquid Concentrate recalled by Diasol | Diasol | Other | Nationwide |
| Device | CLASS II | 100225-10-DEX100, Liquid Concentrate recalled by Diasol | Diasol | Other | Nationwide |
| Device | CLASS II | 100425-10-DEX100, Liquid Concentrate recalled by Diasol | Diasol | Other | Nationwide |
| Device | CLASS II | Kwik-stik, Campylobacter jejuni subsp recalled by Microbiologics | Microbiologics | Other Bacterial Contamination | Nationwide |
| Device | CLASS II | Flexor Check-Flo Introducers and Sets, Reference Part recalled | Cook | Potency & Assay | IN |
| Device | CLASS I | Vapor 2000. Unheated, calibrated anesthetic vaporizer recalled | Draeger | Potency & Assay | Nationwide |
| Device | CLASS II | Affixus Antegrade Femoral Nailing System Affixus Antegrade recalled | Zimmer | Device Malfunction | Nationwide |
| Device | CLASS II | The Stryker CranialMask Tracker is a single-use device recalled | Howmedica Osteonics | Device Malfunction | Nationwide |
| Device | CLASS II | LifeShield Drug Library Management (DLM) recalled by ICU Medical | ICU Medical | Device Malfunction | Nationwide |
| Device | CLASS II | Affixus Antegrade Femoral Nailing System Affixus Antegrade recalled | Zimmer | Device Malfunction | Nationwide |
| Device | CLASS II | Affixus Antegrade Femoral Nailing System Affixus Antegrade recalled | Zimmer | Device Malfunction | Nationwide |
| Device | CLASS II | Restore Clinician Programmer Application (CP App) recalled | Medtronic Neuromodulation | Device Malfunction | Nationwide |
| Device | CLASS II | BD Pyxis MedStation ES recalled by CareFusion 303 | CareFusion 303 | Device Malfunction | Nationwide |
| Drug | CLASS II | Noxafil Powdermix (posaconazole) recalled by Merck Sharp & DohmeNoxafil | Merck Sharp & Dohme | Particulate Matter | Nationwide |
| Drug | CLASS II | Merck Emend (aprepitant) for oral suspension, 125 mg recalledEmend | Merck Sharp & Dohme | Particulate Matter | Nationwide |
| Food | CLASS II | Baby Allergy Herbal Supplement, Contains recalled by A New Life Herbs | A New Life Herbs | Labeling Errors | 12 states |
| Food | CLASS II | Baby Soothe Herbal Supplement, Promotes rest recalled | A New Life Herbs | Labeling Errors | 12 states |
| Food | CLASS II | Traditional Pasta Sauce (meat flavored) recalled by First & Last TavernFirst | First & Last Tavern | Botulism | CT, MA |
| Food | CLASS I | Choceur Cookie Butter Holiday Bark recalled by Silvestri SweetsChoceur | Silvestri Sweets | Undeclared Tree Nuts | Nationwide |
| Food | CLASS II | Boswellia Herbal Supplement, 1:5 Alcohol Double Extract recalledBoswellia | A New Life Herbs | Labeling Errors | 12 states |
| Food | CLASS II | Pain Away Herbal Supplement recalled by A New Life HerbsPain Away | A New Life Herbs | Labeling Errors | 12 states |
| Food | CLASS II | Puttanesca Sauce (olives, capers, hot peppers) recalledFirst | First & Last Tavern | Botulism | CT, MA |
| Food | CLASS II | Grandma Belle's Tomato Basil Soup recalled by Lil TurtlesGrandma Belle's | Lil Turtles | Undeclared Allergens | 14 states |
| Food | CLASS II | Ear Drops Herbal Supplement recalled by A New Life HerbsEar Drops | A New Life Herbs | Labeling Errors | 12 states |
| Food | CLASS II | Zen Cleanse Blend herbal tea recalled by Bell IndustriesZen Cleanse | Bell Industries | Salmonella | MA, TX, WI |
| Food | CLASS I | Choceur Pecan Cranberry & Cinnamon Holiday Bark recalledChoceur | Silvestri Sweets | Undeclared Wheat & Gluten | Nationwide |
| Food | CLASS II | Anti-virus Herbal Supplement, 1:5 Alcohol Tincture recalledAnti-virus | A New Life Herbs | Labeling Errors | 12 states |
| Food | CLASS II | Sinus Cap Herbal Supplement, Herbs containing antibiotic recalledSinus Cap | A New Life Herbs | Labeling Errors | 12 states |
| Food | CLASS II | Marinara Sauce (tomato & basil) recalled by First & Last TavernFirst | First & Last Tavern | Botulism | CT, MA |
| Food | CLASS II | Zimi Puff Pastry French Style (frozen) Package Size and quantity recalledProduct | Karabetian Import and Distribution | Packaging Defects | 10 states |
| Food | CLASS II | Zimi Kunefe Ready to eat (Frozen) Package Size and quantity:/tray recalledProduct | Karabetian Import and Distribution | Packaging Defects | 10 states |
| Food | CLASS II | Ritz Peanut Butter Cracker Sandwiches recalled by Mondelez GlobalRitz | Mondelez Global | Undeclared Allergens | 8 states |
| Food | CLASS II | Chaga Mushroom Herbal Supplement recalled by A New Life HerbsChaga | A New Life Herbs | Labeling Errors | 12 states |
| Food | CLASS II | Organic Ginger Root Herbal Supplement recalled by A New Life Herbs | A New Life Herbs | Labeling Errors | 12 states |
| Food | CLASS II | Publix Raspberry Coffee Cake recalled by The James SkinnerPublix | The James Skinner | Undeclared Tree Nuts | FL |
| Food | CLASS I | Wegmans Deluxe Mixed Nuts, Unsalted recalled by Mellace Family Brands | Mellace Family Brands California | Salmonella | NY, PA |
| Food | CLASS I | Locatelli Pecorino Romano Cheese Grated (Wegmans #270010) Packaged recalledLocatelli Pecorino | Wegmans Food Markets | Listeria | 10 states |
| Food | CLASS I | Ground Beef Products recalled by Mountain West Food Group | Mountain West Food Group | E. coli | |
| Device | CLASS II | Rocket 18Fg Seldinger Catheter with Safety Guard recalled | Rocket Medical | Device Malfunction | 12 states |
| Device | CLASS I | GE Healthcare Carestation anesthesia system Power recalled | GE Medical Systems China | Device Malfunction | Nationwide |
| Device | CLASS II | Halyard, General Laparoscopy Pack recalled by AVID Medical | Avid Medical | Packaging Defects | 4 states |
| Device | CLASS II | AART Gluteal Implant Gluteal Implant recalled by DSAART | Dsaart | Other | 27 states |
| Device | CLASS II | AART Pectoral Implant Pectoral Implant recalled by DSAART | Dsaart | Other | 27 states |
| Device | CLASS II | Intelerad InteleShare recalled by DICOM Grid | Dicom Grid | Labeling Errors | 44 states |
| Device | CLASS II | Forcep, Std Str, Sterile Kelly recalled by Medline Industries | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | of DTT in liquid phase, in PET tube with capture cap, in bulk recalled | Copan Italia | Other | 14 states |
| Device | CLASS II | Scissors, Or, Sharp/blunt, 5.5", Sterile recalled by Medline Industries | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | InPen App recalled by Medtronic MiniMed | Medtronic MiniMed | Device Malfunction | 50 states |
| Device | CLASS II | Orthofix NorthStar OCT Navigation Surgical Technique Guide recalled | Seaspine Orthopedics | Other | 24 states |
| Device | CLASS II | Rocket 12Fg Seldinger Catheter Procedure Tray recalled by Rocket Medical | Rocket Medical | Other | 12 states |
| Device | CLASS II | AART Chin Implant Chin Implant recalled by DSAART | Dsaart | Other | 27 states |
| Device | CLASS II | Zimmer Dermatome recalled by Zimmer Surgical | Zimmer Surgical | Other | OH |
| Device | CLASS II | Xpert¿ Bcr-abl Ultra recalled by Cepheid | Cepheid | Labeling Errors | 27 states |
| Device | CLASS I | GE Healthcare Carestation anesthesia system, product number recalled | GE Medical Systems China | Device Malfunction | Nationwide |
| Device | CLASS II | AART Silicone Carving Implant Silicone Carving Implant recalled | Dsaart | Other | 27 states |
| Device | CLASS II | Rocket 18Fg Seldinger Catheter Procedure Tray recalled by Rocket Medical | Rocket Medical | Device Malfunction | 12 states |
| Device | CLASS II | of DTT in liquid phase, in PET tube with capture cap recalled | Copan Italia | Other | 14 states |
| Device | CLASS II | Rocket 12Fg Seldinger Catheter with Safety Guard recalled | Rocket Medical | Device Malfunction | 12 states |
| Device | CLASS II | 5008X CAREsystem +CLiC +CDX recalled by Fresenius Medical Care | Fresenius Medical Care Holdings | Device Malfunction | LA, MA, MN |
| Device | CLASS I | Ivenix Infusion System (IIS), LVP recalled by Fresenius Kabi USA | Fresenius Kabi USA | Device Malfunction | 20 states |
| Device | CLASS II | Rocket 20Fg Seldinger Catheter Procedure Tray recalled by Rocket Medical | Rocket Medical | Device Malfunction | 12 states |
| Device | CLASS III | Cardiosave Hybrid recalled by Datascope | Datascope | Other | Nationwide |
| Device | CLASS II | AART Malar Implant Malar Implant recalled by DSAART | Dsaart | Other | 27 states |
| Device | CLASS II | Halyard, Head And Neck Tray recalled by AVID Medical | Avid Medical | Packaging Defects | 4 states |
| Device | CLASS II | Halyard, Major Pack recalled by AVID Medical | Avid Medical | Packaging Defects | 4 states |
| Device | CLASS II | AART Calf Implant Calf Implant recalled by DSAART | Dsaart | Other | 27 states |
| Device | CLASS I | GE Healthcare Carestation anesthesia system, product number recalled | GE Medical Systems China | Device Malfunction | Nationwide |
| Device | CLASS III | Cardiosave Rescue recalled by Datascope | Datascope | Other | Nationwide |
| Device | CLASS II | Halyard, EP LAB PK recalled by AVID Medical | Avid Medical | Packaging Defects | 4 states |
| Device | CLASS II | GE HealthCare ViewPoint 6, Catalog Number H47601AA; Radiological recalled | GE Healthcare | Device Malfunction | |
| Device | CLASS II | Rocket 16Fg Seldinger Catheter Procedure Tray recalled by Rocket Medical | Rocket Medical | Device Malfunction | 12 states |
| Device | CLASS II | Halyard, Midtown General Arteriogram recalled by AVID Medical | Avid Medical | Packaging Defects | 4 states |
| Device | CLASS II | Myosa for Kids KS1 recalled by Myofunctional Research | Myofunctional Research Company USA | Other | Nationwide |
| Device | CLASS II | Madsen Accuscreen Teoae/Dpoae/Abr Probe recalled by PATH | Path | Other | WI |
| Device | CLASS II | Hardware configuration of the BeneVision Central Monitoring recalled | Mindray DS USA | Device Malfunction | Nationwide |
| Device | CLASS III | HemosIL SynthAFax recalled by Instrumentation Laboratory | Instrumentation Laboratory | Other | 8 states |
| Device | CLASS II | Biosure HA Screw Threaded metallic bone fixation fastener recalled | Smith & Nephew | Labeling Errors | Nationwide |
| Device | CLASS II | Xpert¿ Bcr-abl Ultra recalled by Cepheid | Cepheid | Labeling Errors | 27 states |
| Drug | CLASS II | Lidocaine HCI 2% and Epinephrine 1:100 recalledLidocaine | Novocol Pharmaceutical of Canada | Packaging Defects | Nationwide |
| Drug | CLASS II | Cook-Walte, Carbocaine 3% (30 mg/mL) recalledCarbocaine | Novocol Pharmaceutical of Canada | Packaging Defects | Nationwide |
| Drug | CLASS III | Cisatracurium Besylate Injection USP, 10 mg/* (2mg/mL) recalledCisatracurium Besylate | Somerset Therapeutics | Potency & Assay | Nationwide |
| Drug | CLASS II | OraVerse, (Phentolamine Mesylate) Injection, 0.4 mg recalledOraverse | Novocol Pharmaceutical of Canada | Packaging Defects | Nationwide |
| Drug | CLASS II | 2% Xylocaine Dental with Epinephrine 1:100 recalledXylocaine | Novocol Pharmaceutical of Canada | Packaging Defects | Nationwide |
| Drug | CLASS III | Cisatracurium Besylate Injection USP, 200mg/*(10mg/mL) recalledCisatracurium Besylate | Somerset Therapeutics | Potency & Assay | Nationwide |
| Drug | CLASS II | 3% Polocaine Dental, Mepivacaine Hydrochloride 3% (30mg/mL) recalledPolocaine | Novocol Pharmaceutical of Canada | Packaging Defects | Nationwide |
| Drug | CLASS II | darby dental supply, Mepivacaine, Mepivacaine HCI recalledMepivacaine | Novocol Pharmaceutical of Canada | Packaging Defects | Nationwide |
| Drug | CLASS II | Ondansetron ODT Tablets, USP 4mg, unit dose tablets, Mfg recalled | Preferred Pharmaceuticals | Packaging Defects | CA |
| Drug | CLASS II | Benco dental Graham Chemical CO., Mepivacaine HCI recalledMepivacaine | Novocol Pharmaceutical of Canada | Packaging Defects | Nationwide |
| Drug | CLASS III | Cisatracurium Besylate Injection USP, 20 mg/*,(2 mg/mL) recalledCisatracurium Besylate | Somerset Therapeutics | Potency & Assay | Nationwide |
| Drug | CLASS II | Ciclopirox Shampoo recalled by Sun Pharma /taro | SUN Pharma /Taro | Potency & Assay | Nationwide |
| Drug | CLASS II | Baclofen Tablets USP, 10 mg recalled by Golden State Medical SupplyBaclofen | Golden State Medical Supply | Other | Nationwide |
| Food | CLASS II | 100% Appleberry Juice recalled by Hollandia DairyHollandia | Hollandia Dairy | Other | CA |
| Food | CLASS I | Food to Live Organic Supergreens Powder Mix recalled by Lexunderto Live | Lexunder | Salmonella | 37 states |
| Food | CLASS II | Chef Milk Pan recalled by Shata TradersChef | Shata Traders | Lead & Heavy Metals | 7 states |
| Food | CLASS II | BaiLiFeng Dried Cinnamon Powder recalled by Good Way Trading GroupBaiLiFeng | Good Way Trading Group | Lead & Heavy Metals | MA |
| Food | CLASS I | Belevini Korushka, Dried Salted Whole Smelts, Net recalled by MamtakimBelevini Korushka | Mamtakim | Botulism | 5 states |
| Food | CLASS I | Food to Live Organic Moringa Leaf Powder, packaged heat-sealed recalledto Live | Lexunder | Salmonella | 37 states |
| Food | CLASS II | Linzer Hearts Baked Cut Out Cookies recalled by Dough-To-GoLinzer Hearts | Dough-To-Go | Undeclared Milk | TN |
| Food | CLASS I | Belevini Bichki, Dried Salted Whole Smelts, Net recalled by MamtakimBelevini Bichki | Mamtakim | Botulism | 5 states |
| Food | CLASS II | Pasteurized Donor Human Milk recalled by The New York Milk BankPasteurized Donor | The New York Milk Bank | Foreign Material | NY |
| Food | CLASS I | Senna Leaves F/c Og recalled by The Whole Herb CompanySenna Leaves | The Whole Herb Company | Salmonella | CA, NJ |
| Food | CLASS II | Celebration Herbals Senna Leaf Herbal Tea 24 Teabags recalledCelebration Herbals | Celebration Herbals Us | Salmonella | 8 states |
| Food | CLASS I | Lorraine Quiche Products recalled by Maître Saladier | Maître Saladier | Foreign Material | |
| Food | CLASS I | Ready-to-Eat Holiday Kielbasa Sausage Products recalled | Olympia Provisions | Foreign Material | |
| Device | CLASS II | BD InLay Optima Ureteral Stent Kit Size:., Ureteral Stent Kit recalled | C.R. Bard | Device Malfunction | Nationwide |
| Device | CLASS III | Forza" PTC Spacer System recalled by Orthofix U.S | Orthofix U.S | Other | Nationwide |
| Device | CLASS III | Pillar" SA PTC Spacer System recalled by Orthofix U.S | Orthofix U.S | Other | Nationwide |
| Device | CLASS I | ErgoStar CM recalled by Draeger | Draeger | Device Malfunction | 10 states |
| Device | CLASS III | Firebird" SI Fusion System recalled by Orthofix U.S | Orthofix U.S | Other | Nationwide |
| Device | CLASS II | Quick Strip Plastic Sterile Adhesive Bandages, 1" x 3", Medline recalled | Medline Industries | Sterility | IL |
| Device | CLASS II | Hemodialysis System, Surdial DX recalled by Nipro Medical | Nipro Medical | Other | Nationwide |
| Device | CLASS II | Medline Perfusion Syringe recalled by Medline Industries | Medline Industries | Device Malfunction | Nationwide |
| Device | CLASS II | Endo Model Knee Fusion Nail SK, Knee Fusion Nail, Coupling Component recalled | Waldemar Link GmbH & Co. KG (Mfg Site) | Other | AL, GA, TX |
| Device | CLASS II | Dexlock Achilles Repair Implant Kits, MAKT4520 recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Stryker MV3 bariatric bed recalled by Stryker Medical Division of | Stryker Medical Division of Stryker | Other | Nationwide |
| Device | CLASS II | Curad Quick Strip Fabric Bandages Containing 30 Bandages recalled | Medline Industries | Sterility | IL |
| Device | CLASS II | Stryker Arise 1000EX mattress recalled by Stryker Medical Division of | Stryker Medical Division of Stryker | Other | Nationwide |
| Device | CLASS II | Senographe Pristina, Pristina Serena, and Pristina Serena 3D recalled | GE Medical Systems | Other | WI |
| Device | CLASS II | Safe-T-Centesis Catheter Drainage Tray recalled | Bard Peripheral Vascular | Other | Nationwide |
| Device | CLASS III | Construx" Mini PTC Spacer System recalled by Orthofix U.S | Orthofix U.S | Other | Nationwide |
| Device | CLASS II | Curad Germ-Shield Touch-Free Fabric Bandages, Sterile recalled | Medline Industries | Sterility | IL |
| Device | CLASS III | Construx" Mini Ti Spacer System recalled by Orthofix U.S | Orthofix U.S | Other | Nationwide |
| Device | CLASS I | ErgoStar CM recalled by Draeger | Draeger | Device Malfunction | 10 states |
| Device | CLASS II | Azurion R3.0 recalled by Philips North America | Philips North America | Other | MA |
| Device | CLASS II | Fur Friends Plastic Sterile Adhesive Bandages, 0.75" x 3", Medline recalled | Medline Industries | Sterility | IL |
| Device | CLASS II | Quick Strip Plastic Sterile Adhesive Bandages, 0.75" x 3", Medline recalled | Medline Industries | Sterility | IL |
| Device | CLASS I | ErgoStar CM recalled by Draeger | Draeger | Device Malfunction | 10 states |
| Device | CLASS II | BD InLay Optima Ureteral Stent Kit Size: 4.., Ureteral Stent Kit recalled | C.R. Bard | Device Malfunction | Nationwide |
| Device | CLASS II | Cardiosave Hybrid recalled by Datascope | Datascope | Other | Nationwide |
| Device | CLASS I | ErgoStar CM recalled by Draeger | Draeger | Device Malfunction | 10 states |
| Device | CLASS II | ChemoPlus gowns recalled by Cardinal Health 200 | Cardinal Health 200 | Labeling Errors | Nationwide |
| Device | CLASS II | Quick Strip Fabric Sterile Adhesive Bandages, 0.75" x 3", Medline recalled | Medline Industries | Sterility | IL |
| Device | CLASS II | Access 2 Reaction Vessels, individual, disposable recalled | Beckman Coulter | Foreign Material | Nationwide |
| Device | CLASS II | Bard InLay Optima Size:., Ureteral Stent Kit recalled by C.R. Bard | C.R. Bard | Device Malfunction | Nationwide |
| Device | CLASS III | Forza" Ti Spacer System recalled by Orthofix U.S | Orthofix U.S | Other | Nationwide |
| Device | CLASS II | BD InLay Optima Ureteral Stent Kit Size:., Ureteral Stent Kit recalled | C.R. Bard | Device Malfunction | Nationwide |
| Device | CLASS II | The Amsco 7053HP Washer/Disinfector is intended for use recalled | Steris | Foreign Material | Nationwide |
| Device | CLASS II | The Amsco 7052HP Washer/Disinfector is intended for use recalled | Steris | Foreign Material | Nationwide |
| Device | CLASS II | Cardiosave Rescue recalled by Datascope | Datascope | Other | Nationwide |
| Device | CLASS II | Quick Strip Fabric Sterile Adhesive Bandages, 1" x 3", Medline recalled | Medline Industries | Sterility | IL |
| Drug | CLASS II | Tropicamide 1%/Cyclopentolate 1%/Phenylephrine recalled | Fagron Compounding Services | Packaging Defects | Nationwide |
| Drug | CLASS III | Nebivolol Tablets, 20 mg recalled by Glenmark PharmaceuticalsNebivolol | Glenmark Pharmaceuticals Inc., USA | Other | Nationwide |
| Drug | CLASS II | Cinacalcet Hydrochloride Tablets, 60 mg recalled by Cipla USACinacalcet | Cipla USA | Nitrosamine Impurity | Nationwide |
| Drug | CLASS II | Lanthanum Carbonate chewable tablets, 1000mg* recalled by Cipla USALanthanum Carbonate | Cipla USA | Potency & Assay | Nationwide |
| Drug | CLASS II | Cinacalcet Hydrochloride Tablets, 30 mg recalled by Cipla USACinacalcet | Cipla USA | Nitrosamine Impurity | Nationwide |
| Drug | CLASS II | Cinacalcet Hydrochloride Tablets, 90 mg recalled by Cipla USACinacalcet | Cipla USA | Nitrosamine Impurity | Nationwide |
| Drug | CLASS II | Sertraline Hydrochloride Tablets USP, 100 mg recalledSertraline Hydrochloride | Lupin Pharmaceuticals | Packaging Defects | Nationwide |
| Drug | CLASS II | Ganirelix Acetate Injection, 250 mcg recalled by Lupin PharmaceuticalsGanirelix Acetate | Lupin Pharmaceuticals | Potency & Assay | 4 states |
| Drug | CLASS III | Morphine Sulfate Oral Solution 100 mg / (20 mg* / mL) recalledMorphine Sulfate | Winder Laboratories | Packaging Defects | Nationwide |
| Drug | CLASS III | Varenicline Tablets, 1mg recalled by Dr. Reddy's LaboratoriesVarenicline Tartrate | Dr. Reddy's Laboratories | Potency & Assay | Nationwide |
| Drug | CLASS II | Lanthanum Carbonate chewable tablets, 1000mg* recalled by Cipla USALanthanum Carbonate | Cipla USA | Potency & Assay | Nationwide |
| Food | CLASS I | Deep-brand Premium Select Green Channa recalled by Chetak New YorkDeep-brand | Chetak New York | Salmonella | NJ |
| Food | CLASS I | Deep-brand Premium Select Chikoo Slices Keep Frozen recalledDeep-brand | Chetak New York | Salmonella | NJ |
| Food | CLASS I | Deep-brand Premium Select Snake Gourd recalled by Chetak New YorkDeep-brand | Chetak New York | Salmonella | NJ |
| Food | CLASS II | Prairie Farms Fat Free Milk plastic jug recalledPrairie | Prairie Farms Dairy | Foreign Material | IL, WI |
| Food | CLASS I | Deep-brand Premium Select Lotus Root (Ring Cut) recalledDeep-brand | Chetak New York | Salmonella | NJ |
| Food | CLASS I | Deep-brand Premium Select Surti Undhiu Mix recalled by Chetak New YorkDeep-brand | Chetak New York | Salmonella | NJ |
| Food | CLASS I | Oven Dried Fish (Scomberomorus Cavalla) recalledOven | African Food on Wheels | Botulism | NY |
| Food | CLASS I | Deep-brand Premium Select Sambhar Mix Keep Frozen recalledDeep-brand | Chetak New York | Salmonella | NJ |
| Food | CLASS I | Deep-brand Ponk With Tangy Sev Keep Frozen recalled by Chetak New YorkDeep-brand Ponk | Chetak New York | Salmonella | NJ |
| Food | CLASS I | Deep-brand Premium Select Jamun Keep Frozen recalled by Chetak New YorkDeep-brand | Chetak New York | Salmonella | NJ |
| Food | CLASS I | Deep-brand Select Val Papdi recalled by Chetak New YorkDeep-brand | Chetak New York | Salmonella | NJ |
| Food | CLASS I | Deep-brand Premium Select Karela Ring Cut Keep Frozen recalledDeep-brand | Chetak New York | Salmonella | NJ |
| Food | CLASS I | Deep-brand Premium Select Surti Papdi Lilva recalled by Chetak New YorkDeep-brand | Chetak New York | Salmonella | NJ |
| Food | CLASS I | Cacio e Pepe Arancini recalled by Stuffed FoodsStuffed | Stuffed Foods | Undeclared Soy | 4 states |
| Food | CLASS I | Sticker label (for Loose Bulk - yellow peaches) recalledSticker | Moonlight Packing | Listeria | 39 states |
| Food | CLASS I | Moonlight Packing products recalledRecalled | Moonlight Packing | Listeria | 39 states |
| Food | CLASS I | ByHeart Whole Nutrition Infant Formula recalled | ByHeart | Botulism | Nationwide |
| Food | CLASS I | Deep-brand Premium Select Green Peas Keep Frozen a) recalledDeep-brand | Chetak New York | Salmonella | NJ |
| Food | CLASS I | Deep-brand Premium Select Surti Papdi Whole recalled by Chetak New YorkDeep-brand | Chetak New York | Salmonella | NJ |
| Food | CLASS I | Sticker label (for Loose Bulk - peppermint peaches) recalledSticker | Moonlight Packing | Listeria | 39 states |
| Food | CLASS I | Deep-brand Premium Select Turmeric Yellow Haldi Keep Frozen recalledDeep-brand | Chetak New York | Salmonella | NJ |
| Food | CLASS I | Deep-brand Premium Select Amla Keep Frozen recalled by Chetak New YorkDeep-brand | Chetak New York | Salmonella | NJ |
| Food | CLASS II | 3 B Cookware recalled by India's Fine Foods | India's Fine Foods | Lead & Heavy Metals | CA, WA |
| Food | CLASS I | Deep-brand Select Chauri recalled by Chetak New YorkDeep-brand | Chetak New York | Salmonella | NJ |
| Food | CLASS I | Deep-brand Select Tindora recalled by Chetak New YorkDeep-brand | Chetak New York | Salmonella | NJ |
| Food | CLASS II | Outer-packaging: gimme! brand Decaf de Agua coffee pods recalledOuter-packaging | Gimme Coffee | Undeclared Allergens | 10 states |
| Food | CLASS I | Sticker label (for Loose Bulk - yellow peaches) recalledSticker | Moonlight Packing | Listeria | 39 states |
| Food | CLASS I | Deep-brand Premium Select Dudhi recalled by Chetak New YorkDeep-brand | Chetak New York | Salmonella | NJ |
| Food | CLASS I | Deep-brand Premium Select Red Guava Slices Keep Frozen recalledDeep-brand | Chetak New York | Salmonella | NJ |
| Food | CLASS I | Deep-brand Premium Select Punjabi Tinda Keep Frozen recalledDeep-brand | Chetak New York | Salmonella | NJ |
| Food | CLASS I | Deep-brand Premium Select Methi Blocks Keep Frozen recalledDeep-brand | Chetak New York | Salmonella | NJ |
| Food | CLASS I | Deep-brand Premium Select Diced Green Mango Keep Frozen recalledDeep-brand | Chetak New York | Salmonella | NJ |
| Food | CLASS I | Deep-brand Premium Select Aviyal Mix Keep Frozen recalledDeep-brand | Chetak New York | Salmonella | NJ |
| Food | CLASS I | Deep-brand Premium Select Red Pearl Onions recalled by Chetak New YorkDeep-brand | Chetak New York | Salmonella | NJ |
| Food | CLASS I | Deep-brand Premium Select Amla Slices Keep Frozen recalledDeep-brand | Chetak New York | Salmonella | NJ |
| Food | CLASS I | Deep-brand Indian Kitchen Quick Cubes Ready recalled by Chetak New YorkDeep-brand | Chetak New York | Salmonella | NJ |
| Food | CLASS I | Deep-brand Premium Select Guvar Keep Frozen a) recalledDeep-brand | Chetak New York | Salmonella | NJ |
| Food | CLASS II | Brass Langri Cookware Sticker label recalled by Santos AgencyBrass Langri | Santos Agency | Lead & Heavy Metals | CA |
| Food | CLASS I | Deep-brand Select Carrots Sliced recalled by Chetak New YorkDeep-brand | Chetak New York | Salmonella | NJ |
| Food | CLASS I | Moonlight Packing products recalledRecalled | Moonlight Packing | Listeria | 39 states |
| Food | CLASS I | Deep-brand Premium Select Methi Chopped Keep Frozen recalledDeep-brand | Chetak New York | Salmonella | NJ |
| Food | CLASS I | Deep-brand Premium Select Singoda (Cooked) Water Chestnuts recalledDeep-brand | Chetak New York | Salmonella | NJ |
| Food | CLASS I | Deep-brand Instant Stuffing For Pani Puri Keep Frozen recalledDeep-brand | Chetak New York | Salmonella | NJ |
| Food | CLASS I | Deep-brand Premium Select Tuvar Lilva recalled by Chetak New YorkDeep-brand | Chetak New York | Salmonella | NJ |
| Food | CLASS I | Deep-brand Premium Select Kantola Keep Frozen recalledDeep-brand | Chetak New York | Salmonella | NJ |
| Food | CLASS II | 3 B Cookware recalled by India's Fine Foods | India's Fine Foods | Lead & Heavy Metals | CA, WA |
| Food | CLASS I | Deep-brand Premium Select Ratalu Sliced Violet Indian Yams recalledDeep-brand | Chetak New York | Salmonella | NJ |
| Food | CLASS I | Deep-brand Select Arvi recalled by Chetak New YorkDeep-brand | Chetak New York | Salmonella | NJ |
| Food | CLASS I | Sticker label (for Loose Bulk - white peaches) recalledSticker | Moonlight Packing | Listeria | 39 states |
| Food | CLASS I | Charlevoix Cheese Company Mild Cheddar Cheese recalledCharlevoix | Boss Dairy Farms | Listeria | MI |
| Food | CLASS I | Moonlight Packing products recalledRecalled | Moonlight Packing | Listeria | 39 states |
| Food | CLASS I | Deep-brand Premium Select Suran recalled by Chetak New YorkDeep-brand | Chetak New York | Salmonella | NJ |
| Food | CLASS II | 3 B Cookware recalled by India's Fine Foods | India's Fine Foods | Lead & Heavy Metals | CA, WA |
| Food | CLASS I | Deep-brand Premium Select Dum Aloo (Cooked) recalled by Chetak New YorkDeep-brand | Chetak New York | Salmonella | NJ |
| Food | CLASS I | Deep-brand Premium Select Green Garlic Keep Frozen recalledDeep-brand | Chetak New York | Salmonella | NJ |
| Food | CLASS I | Moonlight Packing products recalledRecalled | Moonlight Packing | Listeria | 39 states |
| Food | CLASS I | Doughy Chocolate Chip Cookie Dough recalled by Hudson River FoodsDoughy | Hudson River Foods | Salmonella | 15 states |
| Food | CLASS I | Deep-brand Premium Select Fansi Cut French Beans recalledDeep-brand | Chetak New York | Salmonella | NJ |
| Food | CLASS I | Moonlight Packing products recalledRecalled | Moonlight Packing | Listeria | 39 states |
| Food | CLASS I | Deep-brand Premium Select Hot Green Chillies recalled by Chetak New YorkDeep-brand | Chetak New York | Salmonella | NJ |
| Food | CLASS I | Deep-brand Premium Select Tuvar Lilva recalled by Chetak New YorkDeep-brand | Chetak New York | Salmonella | NJ |
| Food | CLASS I | Deep-brand Select Tindora recalled by Chetak New YorkDeep-brand | Chetak New York | Salmonella | NJ |
| Food | CLASS I | Moonlight Packing products recalledRecalled | Moonlight Packing | Listeria | 39 states |
| Food | CLASS I | Deep-brand Premium Select Falsa Keep Frozen recalled by Chetak New YorkDeep-brand | Chetak New York | Salmonella | NJ |
| Food | CLASS I | Deep-brand Indian Kitchen Quick Cubes Ready For Cooking recalledDeep-brand | Chetak New York | Salmonella | NJ |
| Food | CLASS I | Sticker label (for Loose Bulk - peppermint peaches) recalledSticker | Moonlight Packing | Listeria | 39 states |
| Food | CLASS II | Simplot¿ Traditional Reduced Sodium Tater Gems¿ recalled by JR SimplotSimplot | JR Simplot | Foreign Material | 19 states |
| Food | CLASS III | Shloimy's Heimishe Matjes Herring recalled by Kosher FirstShloimy's Heimishe | Kosher First | Undeclared Allergens | NY |
| Food | CLASS I | Deep-brand Premium Select Garlic Cloves recalled by Chetak New YorkDeep-brand | Chetak New York | Salmonella | NJ |
| Food | CLASS I | Deep-brand Premium Select Sweet Corn Keep Frozen recalledDeep-brand | Chetak New York | Salmonella | NJ |
| Food | CLASS I | Deep-brand Premium Select Tapioca (Cassava) Diced Keep Frozen recalledDeep-brand | Chetak New York | Salmonella | NJ |
| Food | CLASS I | Deep-brand Premium Select Baby Bhindi Keep Frozen recalledDeep-brand | Chetak New York | Salmonella | NJ |
| Food | CLASS I | Deep-brand Premium Select Mixed Vegetables 4 way Keep Frozen a) recalledDeep-brand | Chetak New York | Salmonella | NJ |
| Food | CLASS I | Deep-brand Indian Kitchen Quick Cubes Ready For Cooking recalledDeep-brand | Chetak New York | Salmonella | NJ |
| Food | CLASS I | Deep-brand Premium Select Peas and Carrots Keep Frozen recalledDeep-brand | Chetak New York | Salmonella | NJ |
| Food | CLASS I | Deep-brand Select Bhindi Cut Okra Keep Frozen a) recalledDeep-brand | Chetak New York | Salmonella | NJ |
| Food | CLASS I | Ready-To-Eat Frozen Tamales recalled by La Guadalupana | La Guadalupana | Undeclared Allergens | |
| Food | CLASS I | Fully Cooked Breaded Chicken Products recalled by Suzanna's Kitchen | Suzanna's Kitchen | Undeclared Soy | |
| Device | CLASS II | Continuous Glucose Monitor (CGM) recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | IntelliVue MP70 recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Estrogen & Progesterone Test recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | Gut Microbiome Test Medium recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | Vaginal PH Test recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | Environmental Pollutants Profile Test recalled | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | Sorbitol Intolerance Test recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | IBS Test recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | Neurotransmitters XL recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | IntelliVue Patient Monitor MX450 recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Olympus OER-Mini recalled by Aizu Olympus Co | Aizu Olympus | Other | Nationwide |
| Device | CLASS II | Melatonin Test recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | Women s Hormone Test recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | IntelliVue Patient Monitor MX750 recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Fecal Occult Blood Test recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | Epstein-Barr Virus (EBV VCA & EBNA IgG) Test recalled | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | Neurotransmitters Basic recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | IntelliVue Patient Monitor MX550 recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Mammomat Revelation recalled by Siemens Medical Solutions USA | Siemens Medical Solutions USA | Other | Nationwide |
| Device | CLASS II | H pylori (Peptic ulcer) Test recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | Men s Hormone Test recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | Olympus OER-Pro recalled by Aizu Olympus Co | Aizu Olympus | Other | Nationwide |
| Device | CLASS II | Food Sensitivity Test Medium recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | Hemochron Activated Clotting Time Low-Range Test Cuvette recalled | Accriva Diagnostics | Foreign Material | Nationwide |
| Device | CLASS II | IntelliVue Multi-Measurement Module X3 recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Ovulation Test (5 tests) recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | Allergy & Food Intolerance Test recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | Pregnancy Test recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | IntelliVue Patient Monitor MX400 recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Liver Test recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | Diabetes Test (ketones & glucose) recalled | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | Iron Deficiency Test recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | Herpes (Hsv-1 & Hsv-2) Test recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | Thyroid TSH Test recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | Iron Deficiency Test (ferritin) recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | Cholesterol Test recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | Gonorrhea test recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | Reagent Kits/ containing flow cells recalled by Illumina | Illumina | Potency & Assay | Nationwide |
| Device | CLASS II | Chlamydia Test recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | Gut Microbiome Test Large recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | IntelliVue Patient Monitor MX600 recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Hair Mineral Analysis recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | IntelliVue MP20 recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Organic acids Test recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | IntelliVue MP5 recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Drug Test Small (4 substances) recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | Lyme Test recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | Biological Age & Longevity Test recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | IntelliVue MP60 recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | 1 STI Test recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | Blood Type Test recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | Menopause (FSH) 2 Tests recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | 1 Trichomonas / Gardnerella Test recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | Kidney Test recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | Leaky Gut Test recalled by Get Tested International Ab | GET Tested International AB | Packaging Defects | Nationwide |
| Device | CLASS II | InSure ONE Fecal Immunochemical Test recalled by Enterix | Enterix | Other | Nationwide |
| Device | CLASS II | Vitamin D2 and D3 Test recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | NAD Profile Test recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | Food Intolerance Test Large recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | Food Allergy Panel Test (IgE) recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | IntelliVue Multi Measurement Server X2 recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Gut Microbiome Test Mega recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | Female Fertility Test recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | Serotonin Test recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | DHEA Test recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | Sperm Test recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | Parasite Test recalled by Get Tested International Ab | GET Tested International AB | Cyclospora | Nationwide |
| Device | CLASS II | GI Microbiome Profile Small recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | MPOX Test recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | Iodine Test recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | Syphilis Test recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | Candida Test recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | Olympus OER-Elite recalled by Aizu Olympus Co | Aizu Olympus | Other | Nationwide |
| Device | CLASS II | Diabetes HbA1c Test recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | IntelliVue MP40 recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | D-Dimer Test recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | Intestinal Worms Test recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | IntelliVue Patient Monitor MX100 recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | IntelliVue MP80 recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | SIBO Test recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | IntelliVue MP50 recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Trichomonas Vaginalis test recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | Fructose Intolerance Test recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | Incisive CT recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Heavy Metals Test recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | Peptic Ulcer Test (H, pylori) recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | Allergy test Small recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | Food Sensitivity Test Small recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | Mycotoxin Panel Test recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS I | Ivenix Infusion System, Lvp Primary Administration Set recalled | Fresenius Kabi USA | Other | Nationwide |
| Device | CLASS II | Food Sensitivity Test Large recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | IntelliVue MP2 recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Mammomat Fusion recalled by Siemens Medical Solutions USA | Siemens Medical Solutions USA | Other | Nationwide |
| Device | CLASS II | Kwik-stik, Quality control kit for culture media recalled | Microbiologics | Packaging Defects | MN |
| Device | CLASS II | Food Intolerance Test Medium recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | Mammomat Inspiration recalled by Siemens Medical Solutions USA | Siemens Medical Solutions USA | Other | Nationwide |
| Device | CLASS II | Akkermansia Test recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | 1 STI Test Kit recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | Gut Microbiome Test Small recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | IntelliVue Patient Monitor MX850 recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | PSA Test recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | Phantom Fibula Nail, Right, Ti, Fibula Nail recalled by Paragon 28 | Paragon 28 | Potency & Assay | Nationwide |
| Device | CLASS II | Lactose Intolerance Test recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | IntelliVue Patient Monitor MX500 recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Urinary Tract Infection Test recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | CT 5300; Software Version Number recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | IntelliVue Patient Monitor MX700 recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Pet Allergy Test recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | Gut Microbiome Test XL recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | Alcohol (ALC) Test Saliva recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | Ivenix Infusion System (IIS), Large Volume Pump recalled | Fresenius Kabi USA | Device Malfunction | Nationwide |
| Device | CLASS II | Pollen Allergy Test recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | Welch Allyn INF, Thigh 1-Tube recalled by Baxter Healthcare | Baxter Healthcare | Other | Nationwide |
| Device | CLASS II | Neurotransmitters Plus recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | Adrenal Test recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | Parasite Test recalled by Get Tested International Ab | GET Tested International AB | Cyclospora | Nationwide |
| Device | CLASS II | Mycoplasma test, IgG and IgM recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | Sperm Test recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | Lumify Diagnostic Ultrasound System recalled by Philips Ultrasound | Philips Ultrasound | Device Malfunction | Nationwide |
| Device | CLASS II | HPV Antigen Test recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | Illegally Marketed recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | GI Microbiome Profile XL recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | IntelliVue Patient Monitor MX800 recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Allergy test Small recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | Allergy Test IgE recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | Organic Acids Profile Test Large recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | Candida Test recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | Vitamin D-Test recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | IntelliVue MP30 recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Food Intolerance Test Small recalled by Get Tested International Ab | GET Tested International AB | Other | Nationwide |
| Device | CLASS II | IntelliVue MP90 recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Drug | CLASS II | WeCare, Zinc Oxide Ointment recalled by Blossom PharmaceuticalsZinc Oxide | Blossom Pharmaceuticals | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Dynagel, Moisturizing Wound Hydrogel recalled by Blossom Pharmaceuticals | Blossom Pharmaceuticals | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Globe Clotrimazole Cream USP, 1 % Antifungal Cream recalledClotrimazole | Blossom Pharmaceuticals | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Nivagen, Zinc Oxide Ointment recalled by Blossom PharmaceuticalsNivagen Zinc Oxide | Blossom Pharmaceuticals | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Lanashield Skin Barrier, Manfuactured recalled | Blossom Pharmaceuticals | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Globe Clotrimazole Cream, USP, 1 % recalled by Blossom PharmaceuticalsClotrimazole | Blossom Pharmaceuticals | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Phytonadione Injectable Emulsion, USP 10mg/mL recalled by CiplaPhytonadione | Cipla | Potency & Assay | Nationwide |
| Drug | CLASS II | Nivagen, Zinc Oxide Ointment USP, Zinc Oxide 20 % recalledNivagen Zinc Oxide | Blossom Pharmaceuticals | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS III | Carton label: Testosterone Gel 1% per unit dose, Ciii-dose packets recalledTestosterone | Teva Pharmaceuticals USA | Packaging Defects | Nationwide |
| Drug | CLASS II | Dynashield cream recalled by Blossom PharmaceuticalsDynashield | Blossom Pharmaceuticals | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Duloxetine Delayed-Release Capsules, USP, 60 mg recalledDuloxetine | Breckenridge Pharmaceutical | Nitrosamine Impurity | Nationwide |
| Drug | CLASS II | Wecare Calasoothe recalled by Blossom PharmaceuticalsMenthol And Zinc Oxide | Blossom Pharmaceuticals | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Wecare Enema recalled by Blossom PharmaceuticalsSaline Enema | Blossom Pharmaceuticals | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Dynashield Skin Protectant recalled by Blossom PharmaceuticalsDynashield | Blossom Pharmaceuticals | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Duloxetine Delayed-Release Capsules, USP, 60 mg recalledDuloxetine | Breckenridge Pharmaceutical | Nitrosamine Impurity | Nationwide |
| Drug | CLASS II | Phenylephrine HCI, 1000 mcg / Total Volume recalled | Park Avenue Compounding | Manufacturing (CGMP) Deviations | MO |
| Drug | CLASS II | Nivagen Pharmaceuticals, Zinc Oxide Ointment recalledNivagen Zinc Oxide | Blossom Pharmaceuticals | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Haloperidol Lactate Injection, 5 mg/mL recalled by Safecor HealthHaloperidol Lactate | Safecor Health | Packaging Defects | MA |
| Drug | CLASS II | Globe Zinc Oxide Ointment USP Zinc Oxide 20% Skin Protectant recalledZinc Oxide 20% | Blossom Pharmaceuticals | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS III | Bisoprolol Fumarate and Hydrochlorothiazide Tablets recalled | Glenmark Pharmaceuticals Inc., USA | Packaging Defects | Nationwide |
| Food | CLASS II | Food Club Finely Shredded Pizza Style Four Cheese Blend recalled | Great Lakes Cheese Co | Foreign Material | 32 states |
| Food | CLASS II | Costco Item# 19927 Kirkland Signature Caesar Salad, refrigerated recalledCostco Item | Costco Wholesale | Foreign Material | 36 states |
| Food | CLASS II | Pizza style shredded cheese blend recalled by Great Lakes Cheese Co | Great Lakes Cheese Co | Foreign Material | 32 states |
| Food | CLASS I | Sonex aluminum pot recalled by Alanwar FoodSonex | Alanwar Food | Lead & Heavy Metals | NY |
| Food | CLASS I | Organic Moringa Leaf Powder (Moringa Powder) recalled by Africa Imports | Africa Imports | Salmonella | 14 states |
| Food | CLASS II | Italian style shredded cheese blend recalled by Great Lakes Cheese Co | Great Lakes Cheese Co | Foreign Material | 32 states |
| Food | CLASS II | Meadow Gold Hawaii's Dairy Fat Free Chocolate Milk recalledMeadow Gold | Meadowgold Dairies Hawaii | Processing Deviation | HI |
| Food | CLASS II | Lava Bun with Green Tea Flavor bright lime green packaging recalledLava Bun | Prime Food Processing | Undeclared Milk | 33 states |
| Food | CLASS II | Lotsa Pasta International Food Shop Roasted Garlic Infused Olive Oil recalledLotsa | Hale | Botulism | KY |
| Food | CLASS II | Good & Gather Mozzarella & Parmesan shredded cheese blend recalledGood | Great Lakes Cheese Co | Foreign Material | 32 states |
| Food | CLASS II | Onion granules (irradiated) recalled by Laiwu Manhing Vegetables | Laiwu Manhing Vegetables Fruits | Foreign Material | CA |
| Food | CLASS II | Lava Bun with Salted Egg Yolk orange packaging recalledLava Bun | Prime Food Processing | Undeclared Milk | 33 states |
| Food | CLASS III | Coke Farm Beans, Green recalled by Triple BCoke | Triple B | Other | 4 states |
| Food | CLASS I | Dry Roasted Baking Macadamia Nuts, Unsalted Halves Ideal recalledDry | American Nuts | Salmonella | HI |
| Food | CLASS II | Italian Salad Dressing recalled by Ventura Foods | Ventura Foods | Foreign Material | 27 states |
| Food | CLASS II | My Bladder; Supports normal bladder tone & control recalledMy Bladder | Water Pure | E. coli | Nationwide |
| Food | CLASS II | Retail Box: Haagen-Dazs mini chocolate dark chocolate ice recalledRetail Box | Dreyer's Grand Ice Cream | Undeclared Wheat & Gluten | 4 states |
| Food | CLASS II | Aojia Dried Red Bayberry recalled by Rong Shing Trading NYAojia | Rong Shing Trading NY | Undeclared Sulfites | 4 states |
| Food | CLASS III | Prenate Chewable¿ A chewable Rx prenatal vitamin recalledPrenate Chewable | Avion Pharmaceuticals | Undeclared Soy | 17 states |
| Food | CLASS II | Mozzarella and provolone shredded cheese blend recalledMozzarella | Great Lakes Cheese Co | Foreign Material | 32 states |
| Food | CLASS II | Publix Deli Carolina-Style Mustard BBQ Sauce recalled by Ventura FoodsPublix Deli | Ventura Foods | Foreign Material | 27 states |
| Food | CLASS II | Costco Item# 11444 Kirkland Signature Chicken Sandwich with Caesar recalledCostco Item | Costco Wholesale | Foreign Material | 36 states |
| Food | CLASS III | Pacific Seafood Raw Blackened Shrimp Peeled & Deveined recalledPacific Seafood | Pacific Seafood - Portland | Undeclared Sulfites | AL, FL, MA |
| Food | CLASS I | Genepro Whey 4th Generation Plasma Treated Protein, unflavored recalledGenepro Whey | Genepro Protein | Undeclared Milk | 37 states |
| Food | CLASS II | Dojo Asian Wing Sauce, wing sauce hot sauce condiment recalledBlonde Beard's | Blonde Beard's | Undeclared Soy | 31 states |
| Food | CLASS II | Low-moisture part-skim mozzarella shredded cheese, individually recalledLow-moisture | Great Lakes Cheese Co | Foreign Material | 32 states |
| Food | CLASS II | Loaded Veggie Grain Bowl recalled by Nutrition for LongevityLoaded Veggie | Nutrition for Longevity | Listeria | 11 states |
| Food | CLASS II | Happy Farms by Aldi Italian Style shredded cheese blend recalledHappy | Great Lakes Cheese Co | Foreign Material | 32 states |
| Food | CLASS II | Lotsa Pasta International Food Shop Fresh Basil Infused Olive Oil recalledLotsa | Hale | Botulism | KY |
| Food | CLASS I | Fresh Salted Lamb Products recalled by Ghanaianway Restaurant and | Ghanaianway Restaurant and Grocery | Foreign Material | |
| Device | CLASS II | Outlook set utilized in gravity IV administration sets recalled | B Braun Medical | Other | PA |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | Extension Set utilized in gravity IV administration sets recalled | B Braun Medical | Other | PA |
| Device | CLASS II | Camhb W/lhb, Manual, 10/box Ycp112-10 Brucella Broth, 10/box Yt3450 recalled | Remel | Other | Nationwide |
| Device | CLASS II | Anesthesia IV Set utilized in gravity IV administration recalled | B Braun Medical | Other | PA |
| Device | CLASS II | B.Braun utilized in gravity IV administration sets recalled | B Braun Medical | Other | PA |
| Device | CLASS II | NICO Myriad Illumination Pack Product No. NN recalled by Stryker | Stryker | Packaging Defects | Nationwide |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | SafeDAY set utilized in gravity IV administration sets recalled | B Braun Medical | Other | PA |
| Device | CLASS II | Quantum Intersegmental Table recalled by Pivotal Health Solutions | Pivotal Health Solutions | Other | Nationwide |
| Device | CLASS II | Philips Azurion 7M20 systems with FlexArm ceiling-mounted system recalled | Philips Medical Systems Nederl | Packaging Defects | 28 states |
| Device | CLASS II | Blood Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | FlexLab (FLX) recalled by Inpeco | Inpeco | Other | MI |
| Device | CLASS II | Extension Set utilized in gravity IV administration sets recalled | B Braun Medical | Other | PA |
| Device | CLASS II | Burette Set utilized in gravity IV administration sets recalled | B Braun Medical | Other | PA |
| Device | CLASS II | Caresafe utilized in gravity IV administration sets recalled | B Braun Medical | Other | PA |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | Ultrasite set utilized in gravity IV administration sets recalled | B Braun Medical | Other | PA |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | BioFire Respiratory Panel 2.1, IVD recalled by BioFire Diagnostics | BioFire Diagnostics | Device Malfunction | 10 states |
| Device | CLASS II | Catalyft PL & PL40 Expandable Interbody System labeled as recalled | Medtronic Sofamor Danek USA | Other | Nationwide |
| Device | CLASS II | Caresite utilized in gravity IV administration sets recalled | B Braun Medical | Other | PA |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | Outlook set utilized in gravity IV administration sets recalled | B Braun Medical | Other | PA |
| Device | CLASS II | IntelePACS - InteleConnect / TechPortal recalled | Intelerad Medical Systems | Device Malfunction | Nationwide |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | Anesthesia IV Set utilized in gravity IV administration recalled | B Braun Medical | Other | PA |
| Device | CLASS II | Extension Set utilized in gravity IV administration sets recalled | B Braun Medical | Other | PA |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | Anesthesia IV Set utilized in gravity IV administration recalled | B Braun Medical | Other | PA |
| Device | CLASS II | Extension Set utilized in gravity IV administration sets recalled | B Braun Medical | Other | PA |
| Device | CLASS II | The LeadCare¿ II Blood Lead Test System relies recalled | Magellan Diagnostics | Labeling Errors | Nationwide |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | FlexLab (FLX) recalled by Inpeco | Inpeco | Other | MI |
| Device | CLASS I | SJM Pericardial Patch, with EnCap Technology 9x14cm recalled | Glycar SA | Device Malfunction | N/A |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | Evis Exera Iii Duodenovideoscope Olympus Tjf-Q190V recalled | Olympus Corporation of the Americas | Processing Deviation | Nationwide |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | Extension Set utilized in gravity IV administration sets recalled | B Braun Medical | Other | PA |
| Device | CLASS II | Outlook set utilized in gravity IV administration sets recalled | B Braun Medical | Other | PA |
| Device | CLASS II | Anesthesia IV Set utilized in gravity IV administration recalled | B Braun Medical | Other | PA |
| Device | CLASS II | Rate Flow set utilized in gravity IV administration sets recalled | B Braun Medical | Other | PA |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | Cold Form Wrap: Back recalled by DJO | DJO | Packaging Defects | Nationwide |
| Device | CLASS II | Quantum Intersegmental Table recalled by Pivotal Health Solutions | Pivotal Health Solutions | Other | Nationwide |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | ADDitIV utilized in gravity IV administration sets recalled | B Braun Medical | Other | PA |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | FoundationOne Liquid CDx (F1LCDx), Tech recalled by Foundation Medicine | Foundation Medicine | Other | Nationwide |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | Anesthesia IV Set utilized in gravity IV administration recalled | B Braun Medical | Other | PA |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | Extension Set utilized in gravity IV administration sets recalled | B Braun Medical | Other | PA |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS I | SJM Pericardial Patch, with EnCap Technology cm recalled | Glycar SA | Device Malfunction | N/A |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | DermaSensor. Model/Catalog Number: 10101. Software Version recalled | Dermasensor | Device Malfunction | 8 states |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | Outlook set utilized in gravity IV administration sets recalled | B Braun Medical | Other | PA |
| Device | CLASS II | Extension Set utilized in gravity IV administration sets recalled | B Braun Medical | Other | PA |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | Safeline set utilized in gravity IV administration sets recalled | B Braun Medical | Other | PA |
| Device | CLASS II | Constellation Ultravit 10K and Constellation Hypervit 20K recalled | Alcon Research | Other | Nationwide |
| Device | CLASS II | The Anesthesia System is a device used to administer recalled | Mindray DS USA | Packaging Defects | Nationwide |
| Device | CLASS II | Anesthesia IV Set utilized in gravity IV administration recalled | B Braun Medical | Other | PA |
| Device | CLASS II | Anesthesia IV Set utilized in gravity IV administration recalled | B Braun Medical | Other | PA |
| Device | CLASS I | Single Use Ligating Device Olympus HX-400U recalled | Olympus Corporation of the Americas | Other | PA |
| Device | CLASS II | CareLink Clinic recalled by Medtronic MiniMed | Medtronic MiniMed | Device Malfunction | Nationwide |
| Device | CLASS II | Blood Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | Caresite utilized in gravity IV administration sets recalled | B Braun Medical | Other | PA |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | Caresite utilized in gravity IV administration sets recalled | B Braun Medical | Other | PA |
| Device | CLASS II | ADDitIV utilized in gravity IV administration sets recalled | B Braun Medical | Other | PA |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | Emdogain; Article Numbers: 440.230V10, 475.132V10 recalled | Straumann USA | Other | Nationwide |
| Device | CLASS II | Extension Set utilized in gravity IV administration sets recalled | B Braun Medical | Other | PA |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | Option"Elite Vena Cava Filter System recalled by Argon Medical Devices | Argon Medical Devices | Device Malfunction | Nationwide |
| Device | CLASS II | Anesthesia IV Set utilized in gravity IV administration recalled | B Braun Medical | Other | PA |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | Burette Set utilized in gravity IV administration sets recalled | B Braun Medical | Other | PA |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | ADDitIV utilized in gravity IV administration sets recalled | B Braun Medical | Other | PA |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | NN-8000 MHP recalled by Stryker | Stryker | Packaging Defects | Nationwide |
| Device | CLASS II | Extension Set utilized in gravity IV administration sets recalled | B Braun Medical | Other | PA |
| Device | CLASS II | The Anesthesia System is a device used to administer recalled | Mindray DS USA | Packaging Defects | Nationwide |
| Device | CLASS II | NICO BrainPath recalled by Stryker | Stryker | Packaging Defects | Nationwide |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | Extension Set utilized in gravity IV administration sets recalled | B Braun Medical | Other | PA |
| Device | CLASS II | Vista set utilized in gravity IV administration sets recalled | B Braun Medical | Other | PA |
| Device | CLASS II | Blood Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | Outlook set utilized in gravity IV administration sets recalled | B Braun Medical | Other | PA |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | Extension Set utilized in gravity IV administration sets recalled | B Braun Medical | Other | PA |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | Extension Set utilized in gravity IV administration sets recalled | B Braun Medical | Other | PA |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | Xpert MTB/RIF recalled by Cepheid | Cepheid | Potency & Assay | Nationwide |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | FoundationOne CDx (F1CDx), RAL recalled by Foundation Medicine | Foundation Medicine | Other | Nationwide |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | Extension Set utilized in gravity IV administration sets recalled | B Braun Medical | Other | PA |
| Device | CLASS II | Galaxy System recalled by Noah Medical | Noah Medical | Other | 20 states |
| Device | CLASS II | Infusomat utilized in gravity IV administration sets recalled | B Braun Medical | Other | PA |
| Device | CLASS II | Anesthesia IV Set utilized in gravity IV administration recalled | B Braun Medical | Other | PA |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | SafeDAY set utilized in gravity IV administration sets recalled | B Braun Medical | Other | PA |
| Device | CLASS II | Blood Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | IV Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Device | CLASS II | Blood Administration Set utilized recalled by B Braun Medical | B Braun Medical | Other | PA |
| Drug | CLASS II | Dr. Bump Natural Pain Relief Gel, Menthol recalled | CA Botana International | Manufacturing (CGMP) Deviations | 5 states |
| Drug | CLASS II | Walgreens Saline Nasal Spray With Xylitol recalled | Medical Products Laboratories | Sterility | Nationwide |
| Drug | CLASS II | Gabriel Mineral Sunscreen SPF 50, Zinc Oxide 21%, Net per tube recalled | CA Botana International | Manufacturing (CGMP) Deviations | 5 states |
| Drug | CLASS II | Doctor D. Schwab Flawless Skin Fluid Tinted Moisturizer SPF recalled | CA Botana International | Manufacturing (CGMP) Deviations | 5 states |
| Drug | CLASS II | Elixir by Coco March Mineral Sunscreen SPF 50, Zinc Oxide recalled | CA Botana International | Manufacturing (CGMP) Deviations | 5 states |
| Drug | CLASS II | Sea Enzyme Ultra Umbrella Sunscreen SPF recalled | CA Botana International | Manufacturing (CGMP) Deviations | 5 states |
| Drug | CLASS II | Doctor D. Schwab Clinical Weh Natural Pain Relief Gel recalled | CA Botana International | Manufacturing (CGMP) Deviations | 5 states |
| Drug | CLASS II | Clearstem You Are Sunshine Spf 50, Zinc Oxide recalled | CA Botana International | Manufacturing (CGMP) Deviations | 5 states |
| Drug | CLASS II | Doctor. D. Schwab Mineral Sunscreen SPF 50, Zinc Oxide 21% per tube recalled | CA Botana International | Manufacturing (CGMP) Deviations | 5 states |
| Drug | CLASS II | Doctor D. Schwab Shimmery Sun Lotion Sunscreen SPF recalled | CA Botana International | Manufacturing (CGMP) Deviations | 5 states |
| Drug | CLASS II | Doctor D. Schwab Controlling Balm with Tea Tree Oil recalled | CA Botana International | Manufacturing (CGMP) Deviations | 5 states |
| Drug | CLASS I | Famotidine Injection, USP, 20 mg per (10 mg per mL) vials recalledFamotidine | Fresenius Kabi USA | Sterility | Nationwide |
| Drug | CLASS II | Doctor D. Schwab Controlling Cream recalled by CA BOTANA International | CA Botana International | Manufacturing (CGMP) Deviations | 5 states |
| Drug | CLASS II | Sugared+Bronzed Tinted Mineral Sunscreen SPF 50, Zinc Oxide recalled | CA Botana International | Manufacturing (CGMP) Deviations | 5 states |
| Drug | CLASS II | Elixir by Coco March Tinted Mineral Sunscreen SPF recalled | CA Botana International | Manufacturing (CGMP) Deviations | 5 states |
| Drug | CLASS II | Karina Daily Moisturizer SPF 25, Octinoxate 7.5% and Zinc Oxide recalled | CA Botana International | Manufacturing (CGMP) Deviations | 5 states |
| Food | CLASS II | DEVI Cinnamon Powder (Dalchini Powder) recalled by HomeneedsDevi | Homeneeds | Lead & Heavy Metals | WA |
| Food | CLASS I | Whatcom Farmhouse- Sliced recalled by WFM PurchasingWhatcom Farmhouse | WFM Purchasing | E. coli | OR, WA |
| Food | CLASS I | Member's Mark Super Greens Dietary Supplement recalled by MeriCalMember's Mark | MeriCal | Salmonella | Nationwide |
| Food | CLASS II | Jeni's Passion Fruit Dreamsicle Ice Cream Bars recalledJeni's Passion | Jeni's Splendid Ice Creams | Undeclared Allergens | 10 states |
| Food | CLASS I | Face Rock Creamery Vampire Slayer Garlic Cheddar recalled by FRCFace Rock | FRC | Listeria | OR |
| Food | CLASS II | Cinnamon Whiskey Pecans recalled by Nats NutsNat's | Nats Nuts | Undeclared Tree Nuts | 9 states |
| Food | CLASS I | Whatcom Blue Sliced cheese recalled by WFM PurchasingWhatcom | WFM Purchasing | E. coli | OR, WA |