| Food | ANNOUNCED | Kofinas Garlic Mediterranean Infused Extra Virgin Olive Oil recalledKofinas | Lmsi | Hidden Drug Ingredients | |
| Food | ANNOUNCED | Little Temptations Chocolatey Eyeballs recalled by Crystal TemptationsLittle Temptations | Crystal Temptations | Undeclared Milk | 13 states |
| Device | CLASS II | Dentsply Sirona Capsule Mixer recalled by SDI | SDI | Other | 40 states |
| Device | CLASS II | Getinge Y Sensor Module, Servo-u, Servo recalled | Maquet Critical Care AB | Device Malfunction | Nationwide |
| Device | CLASS II | Arrow-LOK Implant recalled by Arrowhead DE | Arrowhead DE | Sterility | Nationwide |
| Device | CLASS II | TD Navio Maxi Speech Generating Device recalled by Tobii Dynavox | Tobii Dynavox | Device Malfunction | Nationwide |
| Device | CLASS II | DxC 500i Clinical Analyzer Modules using recalled by Beckman Coulter | Beckman Coulter | Packaging Defects | Nationwide |
| Device | CLASS II | Innercool Coolblue Console recalled by Gentherm Medical | Gentherm Medical | Other | Nationwide |
| Device | CLASS II | (FDI), Automated Field Steam Sterilizer recalled | Fort Defiance Industries | Other | Nationwide |
| Device | CLASS II | Blanketrol III recalled by Gentherm Medical | Gentherm Medical | Other | Nationwide |
| Device | CLASS I | Enroute Transcarotid Neuroprotection System recalled | Boston Scientific | Other | Nationwide |
| Device | CLASS II | DxC 500 AU Clinical Analyzer Modules using recalled by Beckman Coulter | Beckman Coulter | Packaging Defects | Nationwide |
| Device | CLASS I | BD Needle Kit for Powered Driver recalled by Bard Access Systems | Bard Access Systems | Other | 32 states |
| Device | CLASS II | MiniMed Insulin Pump recalled by Medtronic MiniMed | Medtronic MiniMed | Other | CA |
| Device | CLASS II | Ami HTX recalled by Spectral Instruments | Spectral Instruments | Other | AZ |
| Device | CLASS II | MiniMed Insulin Pump recalled by Medtronic MiniMed | Medtronic MiniMed | Other | CA |
| Device | CLASS II | Lago recalled by Spectral Instruments | Spectral Instruments | Other | AZ |
| Device | CLASS I | Enroute Transcarotid Neuroprotection System Plus recalled | Boston Scientific | Other | Nationwide |
| Device | CLASS III | Custom Made Device Implant 6123 Navicular Cage Nominal Right recalled | Paragon 28 | Other | Nationwide |
| Device | CLASS II | Siemens Healthineers Immulite 2000 Systems SYP Syphilis Screen recalled | Siemens Healthcare Diagnostics Products | Potency & Assay | Nationwide |
| Device | CLASS II | Esteem Body Soft Convex Urostomy recalled by ConvaTec | ConvaTec | Packaging Defects | Nationwide |
| Device | CLASS II | Cardiac Workstation recalled by Philips North America | Philips North America | Labeling Errors | Nationwide |
| Device | CLASS II | EndoFLIP System that includes recalled by Covidien | Covidien | Other | Nationwide |
| Device | CLASS III | Custom Made Device Implant 6123 Navicular Cage Small Right recalled | Paragon 28 | Other | Nationwide |
| Device | CLASS II | Suture Cinch Long Endoscopic tissue approximation device recalled | Boston Scientific | Device Malfunction | Nationwide |
| Device | CLASS II | Siemens Healthineers Immulite 2000 Systems SYP Syphilis Screen recalled | Siemens Healthcare Diagnostics Products | Potency & Assay | Nationwide |
| Device | CLASS II | Cardiac Workstation recalled by Philips North America | Philips North America | Labeling Errors | Nationwide |
| Device | CLASS II | MiniMed Insulin Pump recalled by Medtronic MiniMed | Medtronic MiniMed | Other | CA |
| Device | CLASS II | medical procedure kits and trays labeled as: Crani Pack recalled | American Contract Systems | Sterility | IA, MN, MO |
| Device | CLASS II | Hamilton Microlab STAR Liquid Handler recalled by Foundation Medicine | Foundation Medicine | Device Malfunction | Nationwide |
| Device | CLASS II | Arvis Surgical Navigation System Gen recalled by Kico Knee Innovation | Kico Knee Innovation | Device Malfunction | 19 states |
| Device | CLASS II | TD Navio Midi Speech Generating Device recalled by Tobii Dynavox | Tobii Dynavox | Device Malfunction | Nationwide |
| Device | CLASS II | KidneyVault Portable Renal Perfusion System recalled | Paragonix Technologies | Device Malfunction | Nationwide |
| Device | CLASS II | Syva EMIT 2000 Quinidine Assay recalled | Siemens Healthcare Diagnostics | Potency & Assay | Nationwide |
| Device | CLASS II | Veritas Standard Reverse Total Shoulder Veritas Standard recalled | restor3d | Device Malfunction | Nationwide |
| Device | CLASS II | Blanketrol II recalled by Gentherm Medical | Gentherm Medical | Other | Nationwide |
| Device | CLASS II | Beckman Coulter, Emit 2000 Quinidine Assay recalled | Siemens Healthcare Diagnostics | Potency & Assay | Nationwide |
| Device | CLASS II | medical procedure kits and trays labeled as recalled | American Contract Systems | Sterility | IA, MN, MO |
| Device | CLASS II | One-Piece Guedel Airway, size 00, ISO 5.0, Blue recalled | Intersurgical | Other | Nationwide |
| Device | CLASS II | Halyard Lavh Pack recalled by AVID Medical | Avid Medical | Sterility | Nationwide |
| Device | CLASS II | OverStitch Suture Cinch Endoscopic tissue approximation device recalled | Boston Scientific | Device Malfunction | Nationwide |
| Device | CLASS II | One-Piece Guedel Airway, size 000, ISO 3.5, Light Green recalled | Intersurgical | Other | Nationwide |
| Drug | CLASS II | Tralement (trace elements injection 4*, USP) recalled by American RegentTralement | American Regent | Particulate Matter | Nationwide |
| Drug | CLASS II | Cyanocobalamin injection USP, 1,000 mcg/mL, For IM or SC Use Only recalledCyanocobalamin | American Regent | Particulate Matter | Nationwide |
| Drug | CLASS II | Carbamazepine Tablets, USP, 200mg recalled | SUN Pharmaceutical Industries | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS I | Morphine Sulfate Injection recalled by Fresenius Kabi USAMorphine Sulfate | Fresenius Kabi USA | Packaging Defects | Nationwide |
| Drug | CLASS II | Selenious Acid Injection, USP 12 mcg/ (6 mcg/, For intravenous use recalledSelenious Acid | American Regent | Particulate Matter | Nationwide |
| Drug | CLASS II | Aminaocaproic Acid Injection, USP, 250 mg/mL recalled by American RegentAminocaproic Acid | American Regent | Particulate Matter | Nationwide |
| Drug | CLASS II | niCARdipine Hydrochloride Injection, USP, 25 mg/ (2.5 mg/mL) recalledNicardipine Hydrochloride | American Regent | Particulate Matter | Nationwide |
| Drug | CLASS II | Pemrydi RTU(pemetrexed injection), 500 mg/ (10 mg/mL) recalledPemrydi Rtu | Shilpa Medicare | Other | Nationwide |
| Drug | CLASS II | Acamprosate Calcium, Delayed-Release Tablets, 333 mg recalledAcamprosate Calcium | Mylan Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS II | Nitroglycerin injection, USP, 50 mg/ (5 mg/mL) recalledNitroglycerin | American Regent | Particulate Matter | Nationwide |
| Drug | CLASS II | Libtayo (cemiplimab-rwlc) Injection, 350 mg/ (50 mg/mL) recalledLibtayo | Regeneron Pharmaceuticals | Sterility | Nationwide |
| Drug | CLASS II | Atropine Sulfate injection, USP, 1 mg/mL recalled by American RegentAtropine Sulfate | American Regent | Particulate Matter | Nationwide |
| Drug | CLASS II | Pemrydi RTU (pemetrexed injection), 100 mg/ (10 mg/mL) recalledPemrydi Rtu | Shilpa Medicare | Other | Nationwide |
| Drug | CLASS II | Acetylcysteine Solution, USP, 10% (100 mg/mL) recalledAcetylcysteine | American Regent | Particulate Matter | Nationwide |
| Drug | CLASS I | Papaverine HCl Injection, USP, 60 mg/ (30 mg/mL) recalledPapaverine Hydrochloride | American Regent | Particulate Matter | Nationwide |
| Drug | CLASS II | Acetylcysteine Solution, USP, 20% (200 mg/mL) recalledAcetylcysteine | American Regent | Particulate Matter | Nationwide |
| Drug | CLASS II | Multrys (Trace Elements Injection 4, USP), For intravenous infusion recalledMultrys | American Regent | Particulate Matter | Nationwide |
| Drug | CLASS II | Carbamazepine Tablets, USP, 200mg recalledCarbamazepine | Golden State Medical Supply | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Cyanocobalamin injection USP, 10,000 mcg/ (1,000 mcg/mL) recalledCyanocobalamin | American Regent | Particulate Matter | Nationwide |
| Food | CLASS I | Not Ready-To-Eat Frozen Buffalo Chicken Products recalled | Shanghai Ravioli | Undeclared Allergens | |
| Food | CLASS I | Whole Foods Mango Pineapple Salsa sold as a condiment recalled | WFM Purchasing | Salmonella | 13 states |
| Food | CLASS I | Whole Foods Salsa, Heirloom Tomato recalled by WFM Purchasing | WFM Purchasing | Salmonella | 13 states |
| Food | CLASS I | Jalapeno Pepper recalled by Coast Citrus Distributors | Coast Citrus Distributors | Salmonella | Nationwide |
| Food | CLASS I | Jalapeno Peppers recalled by Get Fresh ProduceGet | Get Fresh Produce | Salmonella | 4 states |
| Food | CLASS I | Vitasia Asian Style Wok Spice Mix recalled by Lidl US TRADINGVitasia Asian | Lidl US TRADING | Salmonella | 10 states |
| Food | CLASS I | Whole Foods Trio Dip, Contains Pico de Gallo, Guacamole, Salsa recalled | WFM Purchasing | Salmonella | 13 states |
| Food | CLASS I | Whole Foods Mild Guacamole Dip, Keep Refrigerated recalled | WFM Purchasing | Salmonella | 13 states |
| Food | CLASS I | Whole Foods Roasted Corn Guacamole Dip, Keep Refrigerated recalled | WFM Purchasing | Salmonella | 13 states |
| Food | CLASS I | Whole Foods Spicy Guacamole Dip No Tomatoes, Keep Refrigerated recalled | WFM Purchasing | Salmonella | 13 states |
| Food | CLASS I | Organic Whole Blueberries recalled by Publix Super Markets | Publix Super Markets | E. coli | 8 states |
| Food | CLASS I | Whole Foods Mild Guacamole Dip No Tomatoes, Keep Refrigerated recalled | WFM Purchasing | Salmonella | 13 states |
| Food | CLASS I | Pepper Jalapeno recalled by Dairyland ProduceDairyland | Dairyland Produce | Salmonella | LA, TX |
| Food | CLASS II | Product is Potato Sourdough Bread recalledProduct | Grand Central Bakery - Oregon | Foreign Material | WA |
| Food | CLASS I | Organic Whole Blueberries recalled by Publix Super Markets | Publix Super Markets | E. coli | 8 states |
| Food | CLASS III | Belgian Chocolate Toffee Gourmet Popcorn recalled by Prospector PopcornProspector | Prospector Popcorn | Labeling Errors | 45 states |
| Food | CLASS II | Chocolate Mocha Gourmet Popcorn recalled by Prospector PopcornProspector | Prospector Popcorn | Labeling Errors | 45 states |
| Food | CLASS I | Organic Whole Mixed Berries recalled by Publix Super Markets | Publix Super Markets | E. coli | 8 states |
| Food | CLASS II | Gifford's HomeMaine ice cream Power Play Fudge recalledGifford's HomeMaine | Gifford's Dairy | Foreign Material | MA, ME, VT |
| Food | CLASS III | Maple Walnut Ice Cream Gourmet Popcorn recalled by Prospector PopcornProspector | Prospector Popcorn | Labeling Errors | 45 states |
| Food | CLASS I | Whole Foods Pomegranate Guacamole Dip, Keep Refrigerated recalled | WFM Purchasing | Salmonella | 13 states |
| Food | CLASS II | Protein Cereal Cocoa Crunch recalled by Nutrient Foods | Nutrient Foods | Undeclared Soy | 10 states |
| Food | CLASS I | Whole Foods Spicy Guacamole Dip, Keep Refrigerated recalled | WFM Purchasing | Salmonella | 13 states |
| Food | CLASS I | Organic Whole Mixed Berries recalled by Publix Super Markets | Publix Super Markets | E. coli | 8 states |
| Food | CLASS III | Fudge Brownie Gourmet Popcorn recalled by Prospector PopcornProspector | Prospector Popcorn | Labeling Errors | 45 states |
| Food | CLASS I | Whole Foods Medium Pico de Gallo Guacamole Dip, Keep Refrigerated recalled | WFM Purchasing | Salmonella | 13 states |
| Device | CLASS II | Biofire Respiratory Panel 2.1 (RP2.1) recalled by BioFire Diagnostics | BioFire Diagnostics | Other | Nationwide |
| Device | CLASS II | ER-Spec Single-Use Vaginal Speculum with LED Light Source, X-Small recalled | OBP Medical | Foreign Material | Nationwide |
| Device | CLASS II | Dermalon 88861757-31 Dermalon* 4-0 Blu C13 recalled by Covidien | Covidien | Sterility | Nationwide |
| Device | CLASS II | Cardinal Health Presource Kits: Basic Pack recalled | Cardinal Health 200 | Other | Nationwide |
| Device | CLASS II | Surgipro SP-623 Surgipro* 2-0 BLU SC2 X36 SP recalled by Covidien | Covidien | Sterility | Nationwide |
| Device | CLASS II | ProNephro AKI (NGAL) Reagent Kit (100 tests) recalled | Bioporto Diagnostics | Potency & Assay | |
| Device | CLASS II | GM Helix Implant, Endosseous Dental Implant Article No. recalled | Straumann USA | Packaging Defects | Nationwide |
| Device | CLASS II | Cardinal Health Presource Kits: Septo Rhino Pack recalled | Cardinal Health 200 | Other | Nationwide |
| Device | CLASS II | Endo-Model, Replacement Set, Tibial Plateau, right/left, L, Uhmwpe recalled | Waldemar Link GmbH & Co. KG (Mfg Site) | Other | IN |
| Device | CLASS II | Non-DEHP Minibore Extension Set RES ME2010 recalled | BD Switzerland Sarl | Sterility | 26 states |
| Device | CLASS II | Xhibit Central Station recalled by Spacelabs Healthcare | Spacelabs Healthcare | Device Malfunction | Nationwide |
| Device | CLASS II | Gore Viabil Short Wire Biliary Endoprosthesis recalled | W L Gore & Associates | Labeling Errors | Nationwide |
| Device | CLASS II | Cardinal Health Presource Kits: Newnan Smr Pack recalled | Cardinal Health 200 | Other | Nationwide |
| Device | CLASS II | Straumann Bone Level Tapered (BLT) Implant, D RC, SLActive recalled | Straumann USA | Other | Nationwide |
| Device | CLASS II | V-Loc 90 Absorbable Wound Closure Device Vloc 90 0 VL recalled | Covidien | Sterility | Nationwide |
| Device | CLASS II | Erbecryo 2 Cryosurgical Unit recalled | Erbe USA | Packaging Defects | Nationwide |
| Device | CLASS II | Philips Azurion recalled by Philips Medical Systems | Philips Medical Systems Nederl | Potency & Assay | |
| Device | CLASS II | Thermo Fisher Diagnostics Neisseria meningitidis Gp C/VL recalled | Remel Europe | Other | Nationwide |
| Device | CLASS II | Medline Micro-Kill Bleach Germicidal Bleach Wipes,7" x 8" recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | navify Digital Pathology (on-prem) v2.5 recalled | Ventana Medical Systems | Device Malfunction | Nationwide |
| Device | CLASS II | Surgipro II S8698GX Surgipro II BL 5/0 18 P-13 S8698GX recalled | Covidien | Sterility | Nationwide |
| Device | CLASS II | Boston Scientific Enhance Transcarotid/Peripheral Access Kit recalled | Galt Medical | Other | Nationwide |
| Device | CLASS I | Baxter Duo-Vent Solution Set and Male Luer Lock Adapter recalled | Baxter Healthcare | Other | Nationwide |
| Device | CLASS I | Elevaris Sodium Chloride Injection recalled by Spectra Medical Devices | Spectra Medical Devices | Foreign Material | 6 states |
| Device | CLASS II | Medline Micro-Kill Bleach Germicidal Bleach Wipes, 6" x 5" recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Medline Micro-Kill Bleach Germicidal Bleach Wipes recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Glidesheath Slender A-kit 6f .021gw recalled by Terumo Medical | Terumo Medical | Packaging Defects | Nationwide |
| Device | CLASS II | Allura Xper FD recalled by Philips Medical Systems | Philips Medical Systems Nederl | Other | Nationwide |
| Device | CLASS II | Medline Micro-Kill Bleach Germicidal Bleach Wipes recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Cardinal Health Presource Kits: Harmonized Spine Vch Phc Pack recalled | Cardinal Health 200 | Other | Nationwide |
| Device | CLASS II | Bobby Balloon Guide Catheter recalled by Microvention | Microvention | Device Malfunction | Nationwide |
| Device | CLASS II | V-Loc 180 Absorbable Wound Closure Device Box Bedside recalled | Covidien | Sterility | Nationwide |
| Device | CLASS II | Gore Viabil Short Wire Biliary Endoprosthesis recalled | W L Gore & Associates | Labeling Errors | Nationwide |
| Drug | CLASS II | Tadalafil USP(1000gm)-bag recalled by Shoolin Pharma Chem L | Shoolin Pharma Chem | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Sildenafil Citrate recalled by Shoolin Pharma Chem L | Shoolin Pharma Chem | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS I | Cefazolin in Dextrose, Injection recalled by Baxter Healthcare | Baxter Healthcare | Particulate Matter | Nationwide |
| Drug | CLASS II | Semaglutide 5mg (1mg/mL), Glycine 25 mg recalled by Apollo Care | Apollo Care | Particulate Matter | Nationwide |
| Drug | CLASS II | Diovan (valsartan) 160 mg recalled by Novartis PharmaceuticalsDiovan | Novartis Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS II | Semaglutide 4.5mg (0.9 mg/mL) Sterile Multi-Dose Vial recalled | Apollo Care | Particulate Matter | Nationwide |
| Drug | CLASS II | Tadalafil USP(500gm)-bag recalled by Shoolin Pharma Chem L | Shoolin Pharma Chem | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Tadalafil USP(100gm)-bag recalled by Shoolin Pharma Chem L | Shoolin Pharma Chem | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Semaglutide 9mg (4.5 mg/mL) Sterile Multi-Dose Vial recalled | Apollo Care | Particulate Matter | Nationwide |
| Drug | CLASS II | Semaglutide 10mg (5mg/mL), Glycine 10 mg recalled by Apollo Care | Apollo Care | Particulate Matter | Nationwide |
| Drug | CLASS II | Semaglutide 20mg (5mg/mL), Glycine 20 mg recalled by Apollo Care | Apollo Care | Particulate Matter | Nationwide |
| Drug | CLASS II | Clear Eyes Maximum Itchy Eye Relief, 0.5 fl oz (15 mL) per dropper recalled | Prestige Brands Holdings | Sterility | Nationwide |
| Drug | CLASS II | Semaglutide 0.9mg (0.9 mg/mL) Sterile Multi-Dose Vial recalled | Apollo Care | Particulate Matter | Nationwide |
| Drug | CLASS II | Semaglutide 6.75mg (4.5 mg/mL) Sterile Multi-Dose Vial recalled | Apollo Care | Particulate Matter | Nationwide |
| Drug | CLASS II | Semaglutide 2.5mg (1mg/mL), Glycine 12.5 mg recalled by Apollo Care | Apollo Care | Particulate Matter | Nationwide |
| Drug | CLASS II | Clindamycin Palmitate Hydrochloride For Oral Solution, USP, 75 mg recalledClindamycin Palmitate Hydrochloride | Heritage Pharmaceuticals | Particulate Matter | Nationwide |
| Drug | CLASS I | Optiray Imaging -350, Ioversol Injection recalledOptiray | Liebel-Flarsheim | Particulate Matter | Nationwide |
| Drug | CLASS II | Semaglutide 2.25MG (0.9 mg/mL) Sterile Multi-Dose Vial recalled | Apollo Care | Particulate Matter | Nationwide |
| Drug | CLASS II | Semaglutide 12.5MG (2.5MG/mL) Sterile Multi-Dose Vial recalled | Apollo Care | Particulate Matter | Nationwide |
| Drug | CLASS I | Glutathione (MDV), 200 mg/mL vial recalled by Victory Medical Center | Victory Medical Center Pharmacy | Sterility | Nationwide |
| Drug | CLASS II | Semaglutide 7.5mg (5mg/mL), Glycine 7.5 mg recalled by Apollo Care | Apollo Care | Particulate Matter | Nationwide |
| Drug | CLASS II | Sildenafil Citrate USP, 100 gm recalled by Shoolin Pharma Chem L | Shoolin Pharma Chem | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS I | Kian Pee Wan Capsules recalled by Buy-Herbal | Buy-Herbal | Labeling Errors | NY |
| Food | CLASS I | Sysco Lettuce Salad Mix 4/5# Sysco Lettuce Salad With Sep recalledSysco | Taylor Farms de Mexico S. de R.L. de C.V | Cyclospora | 27 states |
| Food | CLASS I | Cibus Fresh, Sprig & Sprout, and Jack & Olive brand Garden Salad recalledOlive | Piazza Produce ( | Cyclospora | 6 states |
| Food | CLASS I | Sysco Blend Lett/rom 50/50 Noclr 4/5# Sysco Blend Lett/rom recalledSysco Blend | Taylor Farms de Mexico S. de R.L. de C.V | Cyclospora | 27 states |
| Food | CLASS I | Sysco Lettuce Chop 4/5# Sysco Lettuce Shred 1/8" 4/5# recalledSysco | Taylor Farms de Mexico S. de R.L. de C.V | Cyclospora | 27 states |
| Food | CLASS I | Markon Blend Lett/Rom 80/20 With Sep Baggies 4/5# Iceberg recalledMarkon Blend | Taylor Farms de Mexico S. de R.L. de C.V | Cyclospora | 27 states |
| Food | CLASS I | Aquafaba Powder, Vegan Replacement recalled by 529 CommerceAquafaba | 529 Commerce | Undeclared Egg | 23 states |
| Food | CLASS I | Grade A Brown In-shell Chicken eggs recalledGrade A | Midwest Poultry Servc C/O H & Lelectric | Salmonella | 6 states |
| Food | CLASS I | Peak Lettuce Salad W/Bag 4/5# Iceberg, Carrots, Red Cabbage products recalledPeak | Taylor Farms de Mexico S. de R.L. de C.V | Cyclospora | 27 states |
| Food | CLASS I | Cross Valley Farms Lettuce Chop 4/5# Cross Valley Farms recalledCross Valley | Taylor Farms de Mexico S. de R.L. de C.V | Cyclospora | 27 states |
| Food | CLASS I | Taylor Farms Lettuce Salad W/Bag 4/5# Iceberg, Carrots recalledTaylor | Taylor Farms de Mexico S. de R.L. de C.V | Cyclospora | 27 states |
| Food | CLASS I | Marketside Iceberg Salad recalled by Taylor Farms de Mexico S. deMarketside Iceberg | Taylor Farms de Mexico S. de R.L. de C.V | Cyclospora | 27 states |
| Food | CLASS I | Yum Lettuce Shredded 1/4" 6/5# Iceberg only products recalledYum | Taylor Farms de Mexico S. de R.L. de C.V | Cyclospora | 27 states |
| Food | CLASS I | Cross Valley Farms Blend Lett/Rom 50/50 Noclr 4/5# Cross recalledCross Valley | Taylor Farms de Mexico S. de R.L. de C.V | Cyclospora | 27 states |
| Food | CLASS I | Taylor Farms Lettuce Chop " 4/4# Taylor Farms Lettuce Chop recalledTaylor | Taylor Farms de Mexico S. de R.L. de C.V | Cyclospora | 27 states |
| Food | CLASS I | Markon Lettuce Chop 4/5# Markon Lettuce Shred 1/4" 4/5# recalledMarkon | Taylor Farms de Mexico S. de R.L. de C.V | Cyclospora | 27 states |
| Food | CLASS I | Cross Valley Farms Lettuce Salad Mix 4/5# Cross Valley recalledCross Valley | Taylor Farms de Mexico S. de R.L. de C.V | Cyclospora | 27 states |
| Food | CLASS II | Vodka Tomato Sauce recalled by SheandroVodka | Sheandro | Undeclared Milk | FL |
| Food | CLASS I | Taylor Farms Blend Garden Salad Mix W/rom 6/5# National recalledTaylor | Taylor Farms de Mexico S. de R.L. de C.V | Cyclospora | 27 states |
| Food | CLASS I | Peak Lettuce Shred 1/8" 4/5# Iceberg only products recalledPeak | Taylor Farms de Mexico S. de R.L. de C.V | Cyclospora | 27 states |
| Food | CLASS III | Honeyville Yellow Color Nfi: Water, Fd&c Yellow #5 recalledHoneyville Yellow | FlavorsandColor.Com | Undeclared Allergens | 4 states |
| Food | CLASS I | Markon Blend Lett/Rom 50/50 Noclr 4/5# Markon Blend recalledMarkon Blend | Taylor Farms de Mexico S. de R.L. de C.V | Cyclospora | 27 states |
| Food | CLASS I | Taylor Farms Blend Lett/Rom Blend With Bag 4/5# Iceberg recalledTaylor | Taylor Farms de Mexico S. de R.L. de C.V | Cyclospora | 27 states |
| Food | CLASS I | Dark Chocolate Coconut Almond Bites, 10 Packages recalled by Bazzini | Bazzini | Undeclared Peanuts | WA |
| Food | CLASS I | Subway Shred Lettuce 1/4" 4/5# Iceberg only products recalledSubway Shred | Taylor Farms de Mexico S. de R.L. de C.V | Cyclospora | 27 states |
| Food | CLASS I | Cross Valley Farms Blend Lett/Rom 80/20 With Sep Baggies recalledCross Valley | Taylor Farms de Mexico S. de R.L. de C.V | Cyclospora | 27 states |
| Food | CLASS I | Jack in the Box 1/8" Shred Lettuce 4/5# Iceberg only products recalledJack | Taylor Farms de Mexico S. de R.L. de C.V | Cyclospora | 27 states |
| Food | CLASS I | Markon Lettuce Salad Mix 4/5# Markon Lettuce Salad With Sep recalledMarkon | Taylor Farms de Mexico S. de R.L. de C.V | Cyclospora | 27 states |
| Food | CLASS I | Grade A White In-shell Chicken eggs recalledGrade A | Midwest Poultry Servc C/O H & Lelectric | Salmonella | 6 states |
| Food | CLASS I | Ineligible Siluriformes Fish Products recalled by Asian America Trading | Asian America Trading | Foreign Material | |
| Food | CLASS I | Ready-To-Eat Pickled Goat and Chicken Products recalled by Indus Foods | Indus Foods | Foreign Material | |
| Device | CLASS II | Quantum Rehab Quantum 4Front 2HD recalled by Pride Mobility Products | Pride Mobility Products | Device Malfunction | Nationwide |
| Device | CLASS II | Quantum Rehab Q6 Edge 2.0 (ilevel) recalled by Pride Mobility Products | Pride Mobility Products | Device Malfunction | Nationwide |
| Device | CLASS II | Pkg., Strykeflow Suction/irrigator Ps recalled by Stryker | Stryker | Packaging Defects | Nationwide |
| Device | CLASS II | Quantum Rehab Q6 Edge recalled by Pride Mobility Products | Pride Mobility Products | Device Malfunction | Nationwide |
| Device | CLASS II | Coaptium Connect recalled by Tissium | Tissium | Device Malfunction | Nationwide |
| Device | CLASS II | Ahto Tube Set With Tip Packaging recalled by Stryker | Stryker | Packaging Defects | Nationwide |
| Device | CLASS II | Flow Anesthesia Machine Flow-i C20 6677200 Flow-i C30 recalled | Maquet Critical Care AB | Device Malfunction | Nationwide |
| Device | CLASS II | U2 Total Knee System Femoral offset bushing recalled | United Orthopedic | Device Malfunction | Nationwide |
| Device | CLASS II | Radial Jaw 4 Standard Capacity Biopsy Forceps recalled | Boston Scientific | Sterility | Nationwide |
| Device | CLASS II | Coaptium Connect recalled by Tissium | Tissium | Device Malfunction | Nationwide |
| Device | CLASS II | Merge OrthoPACS, medical imaging diagnostic workstation recalled | Merge Healthcare | Other | Nationwide |
| Device | CLASS II | Kingfisher Compact Individual First Aid Kit recalled | Integrated Medcraft | Other | Nationwide |
| Device | CLASS II | 5-Plasma Bivalirudin Control recalled by Aniara Diagnostica | Aniara Diagnostica | Potency & Assay | Nationwide |
| Device | CLASS II | Coaptium Connect recalled by Tissium | Tissium | Device Malfunction | Nationwide |
| Device | CLASS II | 5-Plasma Bivalirudin Calibrator recalled by Aniara Diagnostica | Aniara Diagnostica | Potency & Assay | Nationwide |
| Device | CLASS II | Intramedullary Bone Saw Blade Assembly recalled by Biomet | Biomet | Sterility | IN |
| Device | CLASS II | Quantum rehab Q6 Edge recalled by Pride Mobility Products | Pride Mobility Products | Device Malfunction | Nationwide |
| Device | CLASS II | Pkg., Single Spike Tube Set recalled by Stryker | Stryker | Packaging Defects | Nationwide |
| Device | CLASS III | Syva Emit Disopyramide Assay Enzyme Immunoassay recalled | Siemens Healthcare Diagnostics | Potency & Assay | Nationwide |
| Device | CLASS II | Neuroguard IEP 1 Carotid Stent recalled by Contego Medical | Contego Medical | Device Malfunction | Nationwide |
| Device | CLASS II | The GEM Premier 7000 with iQM3 is a portable critical care recalled | Instrumentation Laboratory | Device Malfunction | Nationwide |
| Device | CLASS I | Halyard convenience kits containing Medline Namic recalled | Avid Medical | Particulate Matter | Nationwide |
| Device | CLASS II | Philips Allura, Cardio Vascular-Allura Centron recalled | Philips Medical Systems Nederl | Other | Nationwide |
| Device | CLASS II | REF # D23352, MicroScan LabPro V5.03 Panel Update 11 (US) recalled | Beckman Coulter | Other | Nationwide |
| Device | CLASS II | DASH Rapid PCR Instrument recalled by Nuclein | Nuclein | Device Malfunction | Nationwide |
| Device | CLASS II | Charger for the Therabody Theragun, G4 PRO massage device recalled | Therabody | Device Malfunction | Nationwide |
| Device | CLASS II | Remisol Advance recalled by Beckman Coulter Biomedical | Beckman Coulter Biomedical | Potency & Assay | 5 states |
| Device | CLASS II | Quantum Rehab Q6 Edge recalled by Pride Mobility Products | Pride Mobility Products | Device Malfunction | Nationwide |
| Device | CLASS II | Medical Action Industries Dialysis Change Tray Clear Sequence recalled | Medical Action Industries Inc. 306 | Packaging Defects | Nationwide |
| Device | CLASS II | Quantum Rehab R-trak recalled by Pride Mobility Products | Pride Mobility Products | Device Malfunction | Nationwide |
| Device | CLASS II | Intramedullary Bone Saw Blade Assembly recalled by Biomet | Biomet | Sterility | IN |
| Device | CLASS II | Coaptium Connect recalled by Tissium | Tissium | Device Malfunction | Nationwide |
| Device | CLASS II | HardyDisk AST Cefiderocol 30¿g (FDC30) recalled by Hardy Diagnostics | Hardy Diagnostics | Other | Nationwide |
| Device | CLASS II | Quantum Rehab Quantum Rival recalled by Pride Mobility Products | Pride Mobility Products | Device Malfunction | Nationwide |
| Device | CLASS II | Quantum Rehab Q6 Edge HD recalled by Pride Mobility Products | Pride Mobility Products | Device Malfunction | Nationwide |
| Device | CLASS II | Coaptium Connect recalled by Tissium | Tissium | Device Malfunction | Nationwide |
| Device | CLASS II | FilmArray NGDS Warrior Panel recalled by Biofire Defense | Biofire Defense | Device Malfunction | Nationwide |
| Device | CLASS I | Infinion Cx Lead Kit recalled by Boston Scientific | Boston Scientific Neuromodulation | Other | NY |
| Device | CLASS II | Quantum Rehab Quantum recalled by Pride Mobility Products | Pride Mobility Products | Device Malfunction | Nationwide |
| Device | CLASS II | Quantum Rehab 4Front recalled by Pride Mobility Products | Pride Mobility Products | Device Malfunction | Nationwide |
| Device | CLASS II | Intramedullary Bone Saw Blade Assembly recalled by Biomet | Biomet | Sterility | IN |
| Device | CLASS II | Merge PACS, medical imaging diagnostic workstation recalled | Merge Healthcare | Other | Nationwide |
| Device | CLASS II | Intramedullary Bone Saw Blade Assembly recalled by Biomet | Biomet | Sterility | IN |
| Device | CLASS II | U2 Total Knee System Femoral valgus offset adaptor, left recalled | United Orthopedic | Device Malfunction | Nationwide |
| Device | CLASS II | Drive and munevo Drive r-net Powered Wheelchair Hands-Free recalled | Munevo | Device Malfunction | Nationwide |
| Device | CLASS II | Radial Jaw 4 Large Capacity Biopsy Forceps recalled by Boston Scientific | Boston Scientific | Sterility | Nationwide |
| Device | CLASS II | Coaptium Connect recalled by Tissium | Tissium | Device Malfunction | Nationwide |
| Device | CLASS II | Intramedullary Bone Saw Blade Assembly recalled by Biomet | Biomet | Sterility | IN |
| Device | CLASS II | Quantum Rehab Quantum 4Front recalled by Pride Mobility Products | Pride Mobility Products | Device Malfunction | Nationwide |
| Device | CLASS II | GE Healthcare Portrait Core Services SW recalled by GE Medical Systems | GE Medical Systems Information Technologies | Device Malfunction | Nationwide |
| Device | CLASS II | Nerivio Infinity recalled by Theranica Bioelectronics | Theranica Bioelectronics | Device Malfunction | |
| Device | CLASS I | Halyard convenience kits containing Medline Namic recalled | Avid Medical | Particulate Matter | Nationwide |
| Device | CLASS II | Ahto Tube Set Packaging recalled by Stryker | Stryker | Packaging Defects | Nationwide |
| Device | CLASS II | Anti-Torque, Vector, Part: LS-749 part of Vector Pedicle recalled | Innovasis | Other | Nationwide |
| Device | CLASS II | Ustar II Knee System Hinge Box Trial, L, #1 recalled | United Orthopedic | Device Malfunction | Nationwide |
| Device | CLASS II | Ahto Dual Spike Tube Set Packaging recalled by Stryker | Stryker | Packaging Defects | Nationwide |
| Device | CLASS II | GEM Premier 5000 PAK Part Numbers recalled by Instrumentation Laboratory | Instrumentation Laboratory | Device Malfunction | Nationwide |
| Device | CLASS II | Coaptium Connect recalled by Tissium | Tissium | Device Malfunction | Nationwide |
| Device | CLASS II | 5-Plasma Bivalirudin AMR Verification Kit recalled by Aniara Diagnostica | Aniara Diagnostica | Potency & Assay | Nationwide |
| Device | CLASS II | Brand Name: WASPLab Product Name: WASPLab Model/Catalog Number: W087 recalled | Copan Wasp | Device Malfunction | Nationwide |
| Device | CLASS II | Pre-loved SNOO Smart Sleeper recalled by Happiest Baby | Happiest Baby | Other | Nationwide |
| Device | CLASS II | Coaptium Connect recalled by Tissium | Tissium | Device Malfunction | Nationwide |
| Device | CLASS II | Quantum Rehab Quantum Outback recalled by Pride Mobility Products | Pride Mobility Products | Device Malfunction | Nationwide |
| Device | CLASS II | Quantum Rehab Q6 Edge 3 Stretto recalled by Pride Mobility Products | Pride Mobility Products | Device Malfunction | Nationwide |
| Device | CLASS II | U2 Total Knee System PSA Box Trial, L, #1 recalled by United Orthopedic | United Orthopedic | Device Malfunction | Nationwide |
| Device | CLASS II | Radial Jaw 4 Jumbo Biopsy Forceps recalled by Boston Scientific | Boston Scientific | Sterility | Nationwide |
| Device | CLASS I | Halyard convenience kits containing Medline Namic recalled | Avid Medical | Particulate Matter | Nationwide |
| Device | CLASS II | U2 Total Knee System Femoral offset bushing recalled | United Orthopedic | Device Malfunction | Nationwide |
| Device | CLASS II | Blom-Singer Classic Indwelling Voice Prosthesis recalled | Freudenberg Medical | Labeling Errors | Nationwide |
| Device | CLASS II | Blom-Singer Classic Indwelling Voice Prosthesis recalled | Freudenberg Medical | Labeling Errors | Nationwide |
| Device | CLASS II | REF # D23354, MicroScan LabPro V5.03 Panel Update 11 DVD Kit (US) recalled | Beckman Coulter | Other | Nationwide |
| Device | CLASS II | GE Healthcare MAC VU360 recalled by GE Medical Systems | GE Medical Systems Information Technologies | Device Malfunction | Nationwide |
| Device | CLASS II | Forward Oral Airway Kit (OPA Sizes 5, 6.5, 7 recalled | Integrated Medcraft | Other | Nationwide |
| Device | CLASS II | MC2 Portable X-Ray System recalled by Oxos Medical | Oxos Medical | Device Malfunction | Nationwide |
| Device | CLASS II | Atellica CH Urine Albumin recalled by Siemens Healthcare Diagnostics | Siemens Healthcare Diagnostics | Potency & Assay | Nationwide |
| Device | CLASS II | U2 Total Knee System Femoral valgus adaptor, left and right recalled | United Orthopedic | Device Malfunction | Nationwide |
| Device | CLASS III | Syva Emit tox Serum Tricyclic Antidepressant recalled | Siemens Healthcare Diagnostics | Potency & Assay | Nationwide |
| Drug | CLASS I | Cyclophosphamide for Injection, USP, One Single-Dose Vial recalled | Sunny Pharmtech | Particulate Matter | Nationwide |
| Drug | CLASS II | Mirabegron Extended-Release Tablets, 25 mg recalledMirabegron | Zydus Pharmaceuticals | Nitrosamine Impurity | Nationwide |
| Drug | CLASS III | Total Parental Nutrition - Pediatric PN Patient-Specific recalled | Central Admixture Pharmacy Services | Packaging Defects | GA |
| Drug | CLASS I | Cyclophosphamide for Injection, USP, One Single-Dose Vial recalled | Sunny Pharmtech | Particulate Matter | Nationwide |
| Drug | CLASS II | Dicyclomine Hydrochloride Capsules, USP, 10mg recalledDicyclomine Hydrochloride | Aurobindo Pharma USA | Packaging Defects | Nationwide |
| Food | CLASS I | LLP, sharp cheese variety (Cheddar, Yummy Cheddar recalledClover Hill | Clover Hill Dairy | Listeria | MD, NY, VA |
| Food | CLASS II | Ultimate Mother's Day Wangshin Doenjang Aged 3 Years Korean recalledUltimate Mother's | Jina F&c | Undeclared Allergens | |
| Food | CLASS I | Requeson, bulk product from Clover Hill Dairy packed into recalledRequeson | La Colonia Foods | Listeria | MD, VA |
| Food | CLASS I | LLP, Flavored Cheese (horseradish) recalled by Clover Hill DairyClover Hill | Clover Hill Dairy | Listeria | MD, NY, VA |
| Food | CLASS I | Salvadoreno Requeson Soft Ricotta recalled by La Colonia FoodsLa Colonia | La Colonia Foods | Listeria | MD, VA |
| Food | CLASS I | LLP, Cuajada (vacuum sealed) recalled by Clover Hill DairyClover Hill | Clover Hill Dairy | Listeria | MD, NY, VA |
| Food | CLASS I | Selectos Latinos Requeson Salvadoreno Ricotta Style recalledSelectos Latinos | La Colonia Foods | Listeria | MD, VA |
| Food | CLASS III | Kanni Delight 31/40 Fresh Frozen Vannamei White Shrimp IQF recalledKanni Delight | Campo Rico Foods | Packaging Defects | LA |
| Food | CLASS I | LLP, Mild Cheese Variety-a-pack assorted White Colby recalledClover Hill | Clover Hill Dairy | Listeria | MD, NY, VA |
| Food | CLASS I | LLP, Smoked Cheddar Cheese Varieties (Cheddar, White Cheddar) recalledClover Hill | Clover Hill Dairy | Listeria | MD, NY, VA |
| Food | CLASS I | LLP, Soft Cuajada (vacuum sealed) recalled by Clover Hill DairyClover Hill | Clover Hill Dairy | Listeria | MD, NY, VA |
| Food | CLASS II | "***Hondashi***" seasoning recalled by Pack'n Fresh | Pack'n Fresh | Undeclared Allergens | CA, NJ |
| Food | CLASS I | LLP, Soft Cuajada crumbs recalled by Clover Hill DairyClover Hill | Clover Hill Dairy | Listeria | MD, NY, VA |
| Food | CLASS I | Blank Slate Creamery Vegan Non-dairy Frozen Dessert Coconut recalledBlank Slate | Blank Slate Creamery Production | Undeclared Egg | MI |
| Food | CLASS II | Sliced Korean Halibut with Soy sauce, Wasabi, Vinegar Chili Paste recalled | Eunha Fisheries Co | Undeclared Wheat & Gluten | CA, NJ |
| Food | CLASS I | LLP, Smoked Pepper Cheese Varieties (Jalapeno Cheddar) recalledClover Hill | Clover Hill Dairy | Listeria | MD, NY, VA |
| Food | CLASS II | Flounder Sashimi With Sauce recalled by Eunha Fisheries CoFlounder Sashimi | Eunha Fisheries Co | Undeclared Wheat & Gluten | CA, NJ |
| Food | CLASS II | Big Way Hot Pot "Hot Pot Miso Paste"; unit package recalledBig Way | Big Way Ca | Undeclared Milk | CA |
| Food | CLASS I | Ashfiat Alharamain Energy Support recalled by AkkarcoAshfiat Alharamain | Akkarco | Undeclared Allergens | Nationwide |
| Food | CLASS I | LLP, Flavored Cheese (Old Bay Cheddar) recalled by Clover Hill DairyClover Hill | Clover Hill Dairy | Listeria | MD, NY, VA |
| Food | CLASS II | Flexible food pouch (3-layer foil, spouted, #CP6088) recalledFlexible | Cheer Pack | Foreign Material | OR |
| Food | CLASS I | LLP, mild cheese variety (Fresh Cheddar Curd) recalledClover Hill | Clover Hill Dairy | Listeria | MD, NY, VA |
| Food | CLASS I | LLP, Soft Ricotta (Requeson), and Soft Ricotta recalledClover Hill | Clover Hill Dairy | Listeria | MD, NY, VA |
| Food | CLASS I | LLP, Pepper Jack Cheese Varieties-a-Pack Assorted Jalapeno recalledClover Hill | Clover Hill Dairy | Listeria | MD, NY, VA |
| Food | CLASS I | KC Everyday Mac & Cheese recalled by KerryKC Everyday | Kerry | Undeclared Allergens | 5 states |
| Food | CLASS I | LLP, Sharp Cheese Snack Pack Sharp Stix White or Yellow recalledClover Hill | Clover Hill Dairy | Listeria | MD, NY, VA |
| Food | CLASS I | LLP, Soft Cuajada in Brine recalled by Clover Hill DairyClover Hill | Clover Hill Dairy | Listeria | MD, NY, VA |
| Food | CLASS II | Pumpkin Tree Peter Rabbit Organics Banana & Strawberry fruit puree recalledPumpkin Tree | PT Organics | Foreign Material | 23 states |
| Food | CLASS I | LLP, Pepper Jack Cheese Varieties recalled by Clover Hill DairyClover Hill | Clover Hill Dairy | Listeria | MD, NY, VA |
| Food | CLASS I | LLP, Mild Cheese Variety (Yummy Cheddar, White Cheddar recalledClover Hill | Clover Hill Dairy | Listeria | MD, NY, VA |
| Food | CLASS I | Zen Principle Naturals Moringa Leaf Powder dietary recalled by Factory6Zen Principle | Factory6 | Salmonella | NV |
| Food | CLASS I | LLP, Pepper Jack Cheese Varieties (Jalapeno Cheddar recalledClover Hill | Clover Hill Dairy | Listeria | MD, NY, VA |
| Food | CLASS I | Spicy Breakfast Burrito sold under the following products recalledfollowing | M.G. Foods | Undeclared Soy | 8 states |
| Food | CLASS I | LLP, mild cheese variety (Snack Pack Assorted Regular Mild recalledClover Hill | Clover Hill Dairy | Listeria | MD, NY, VA |
| Food | CLASS I | Selectos Latinos Requeson Mexicano Mexican Cottage Cheese recalledSelectos Latinos | La Colonia Foods | Listeria | MD, VA |
| Food | CLASS I | Ready-To-Eat Pastrami and Corned Beef Products recalled | City Foods, Inc./Bea's Best Corned Beef | Listeria | |
| Food | HEALTH ALERT | Various Meat and Poultry Products Containing FDA-Regulated recalled | FSIS | Salmonella | |
| Food | CLASS I | Raw Beef Products recalled by Corte Argentino USA | Corte Argentino USA | Processing Deviation | |
| Food | CLASS I | Ineligible Frozen Siluriformes Breaded Fish Fillet recalled | Shan Distribution Network | Processing Deviation | |
| Device | CLASS II | GEM Premier recalled by Instrumentation Laboratory | Instrumentation Laboratory | Other | Nationwide |
| Device | CLASS II | L-Cath PICC S/L Peripherally Inserted Central Catheter: (1.9F) recalled | Argon Medical Devices | Labeling Errors | 28 states |
| Device | CLASS II | Hoffmann II Connecting Rod Micro recalled by Stryker | Stryker | Sterility | Nationwide |
| Device | CLASS II | Eopa Elongated One-Piece Arterial Cannula Blunt recalled | Medtronic Perfusion Systems | Packaging Defects | Nationwide |
| Device | CLASS II | GEM Premier 5000 with IQM2 recalled by Instrumentation Laboratory | Instrumentation Laboratory | Other | Nationwide |
| Device | CLASS II | Ams Aligned Medical Solutions medical convenience kits recalled | Windstone Medical Packaging | Sterility | Nationwide |
| Device | CLASS II | Ams Aligned Medical Solutions medical convenience kits recalled | Windstone Medical Packaging | Packaging Defects | Nationwide |
| Device | CLASS II | Ams Aligned Medical Solutions medical convenience kits recalled | Windstone Medical Packaging | Packaging Defects | Nationwide |
| Device | CLASS I | Pack Angiography Ncmc 3/Cs Banner recalled by Medical Action Industries | Medical Action Industries Inc. 306 | Particulate Matter | AZ, CO |
| Device | CLASS II | M5 Corpus Power Wheelchair recalled by Permobil | Permobil | Other | Nationwide |
| Device | CLASS II | Hoffmann II Connecting Rod Micro recalled by Stryker | Stryker | Sterility | Nationwide |
| Device | CLASS II | Ingenuity CT CT5000 Ingenuity Plus CT5000 Ingenuity Pro recalled | Philips Medical Systems | Device Malfunction | Nationwide |
| Device | CLASS II | Ams Aligned Medical Solutions medical convenience kits recalled | Windstone Medical Packaging | Packaging Defects | Nationwide |
| Device | CLASS II | Hoffmann II Connecting Rod Micro recalled by Stryker | Stryker | Sterility | Nationwide |
| Device | CLASS II | Hoffmann II Connecting Rod Micro recalled by Stryker | Stryker | Sterility | Nationwide |
| Device | CLASS II | Brilliance iCT Brilliance iCT Upgrades Brilliance iCT SP recalled | Philips Medical Systems | Device Malfunction | Nationwide |
| Device | CLASS II | M3 Corpus Power Wheelchair with Heavy Duty Shock recalled by Permobil | Permobil | Potency & Assay | Nationwide |
| Device | CLASS II | EOPA Elongated One-Piece Arterial Cannula DIL TIP recalled | Medtronic Perfusion Systems | Packaging Defects | Nationwide |
| Device | CLASS II | Eopa Elongated One-Piece Arterial Cannula Blunt recalled | Medtronic Perfusion Systems | Packaging Defects | Nationwide |
| Device | CLASS II | Ams Aligned Medical Solutions medical convenience kits recalled | Windstone Medical Packaging | Sterility | Nationwide |
| Device | CLASS II | GEM Premier 7000 with iQM3 recalled by Instrumentation Laboratory | Instrumentation Laboratory | Other | Nationwide |
| Device | CLASS II | L-Cath Midline S/L Catheter (3F) recalled by Argon Medical Devices | Argon Medical Devices | Labeling Errors | 28 states |
| Device | CLASS II | EOPA 3D Arterial Cannula DIL TIP, intended for use recalled | Medtronic Perfusion Systems | Packaging Defects | Nationwide |
| Device | CLASS II | Ams Aligned Medical Solutions medical convenience kits recalled | Windstone Medical Packaging | Sterility | Nationwide |
| Device | CLASS II | EOPA 3D Arterial Cannula, intended for use recalled | Medtronic Perfusion Systems | Packaging Defects | Nationwide |
| Device | CLASS II | IQon Spectral CT IQon Spectral CT Upgrades recalled | Philips Medical Systems | Device Malfunction | Nationwide |
| Device | CLASS II | Power Over Fiber Base Module recalled by Terex Utilities | Terex Utilities | Other | Nationwide |
| Device | CLASS II | Ams Aligned Medical Solutions medical convenience kits recalled | Windstone Medical Packaging | Packaging Defects | Nationwide |
| Device | CLASS II | Ams Aligned Medical Solutions medical convenience kits recalled | Windstone Medical Packaging | Packaging Defects | Nationwide |
| Device | CLASS II | Hoffmann II Connecting Rod Micro recalled by Stryker | Stryker | Sterility | Nationwide |
| Device | CLASS II | Ams Aligned Medical Solutions medical convenience kits recalled | Windstone Medical Packaging | Packaging Defects | Nationwide |
| Device | CLASS II | GEM Premier recalled by Instrumentation Laboratory | Instrumentation Laboratory | Other | Nationwide |
| Device | CLASS II | OsteoBallast, . (SeaSpine Brand) recalled by IsoTis OrthoBiologicsSeaSpine | IsoTis OrthoBiologics | Other | Nationwide |
| Device | CLASS II | Ams Aligned Medical Solutions medical convenience kits recalled | Windstone Medical Packaging | Sterility | Nationwide |
| Device | CLASS I | Astral 100/150 Resmed Astral 100/50 is a ventilator system recalled | ResMed | Packaging Defects | Nationwide |
| Device | CLASS II | GEM Premier recalled by Instrumentation Laboratory | Instrumentation Laboratory | Other | Nationwide |
| Device | CLASS II | Hoffmann II Connecting Rod Micro recalled by Stryker | Stryker | Sterility | Nationwide |
| Device | CLASS II | EOPA Elongated One-Piece Arterial Cannula DIL TIP recalled | Medtronic Perfusion Systems | Packaging Defects | Nationwide |
| Device | CLASS II | Hoffmann II Connecting Rod Micro recalled by Stryker | Stryker | Sterility | Nationwide |
| Device | CLASS II | GEM Premier recalled by Instrumentation Laboratory | Instrumentation Laboratory | Other | Nationwide |
| Device | CLASS II | Ams Aligned Medical Solutions medical convenience kits recalled | Windstone Medical Packaging | Packaging Defects | Nationwide |
| Device | CLASS II | Ams Aligned Medical Solutions medical convenience kits recalled | Windstone Medical Packaging | Packaging Defects | Nationwide |
| Drug | CLASS III | Dabigatran Etexilate Capsules, 150 mg recalled by Ascend LaboratoriesDabigatran Etexilate | Ascend Laboratories | Potency & Assay | Nationwide |
| Drug | CLASS II | Dorzolamide HCl and Timolol Maleate Ophthalmic Solution recalledDorzolamide Hydrochloride And Timolol Maleate Ophthalmic Solution | Micro Labs USA | Other | Nationwide |
| Drug | CLASS II | Mycophenolate Mofetil for Injection USP, 500 mg/Vial recalledMycophenolate Mofetil | Mylan Pharmaceuticals | Other | Nationwide |
| Drug | CLASS II | Azelaic Acid Gel, 15% tubes, For Topical Use only recalledAzelaic Acid | Glenmark Pharmaceuticals Inc., USA | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS III | Dabigatran Etexilate Capsules, 75 mg recalled by Ascend LaboratoriesDabigatran Etexilate | Ascend Laboratories | Potency & Assay | Nationwide |
| Drug | CLASS III | Dabigatran Etexilate Capsules, 75 mg recalled by Ascend LaboratoriesDabigatran Etexilate | Ascend Laboratories | Potency & Assay | Nationwide |
| Food | CLASS II | Super Skin; Dietary Supplement;, 2 per day recalled by Mellish IslandMellish Island | Mellish Island | Other | Nationwide |
| Food | CLASS I | Requeson (soft ricotta) packed into a package recalledRequeson | Nelson & Isa Lacteos | Listeria | NY |
| Food | CLASS II | DQ Chocolate Reduced Fat Ice Cream Mix recalled by Galliker Dairy Co | Galliker Dairy Co | Foreign Material | 5 states |