| Device | CLASS II | True 3D Viewer recalled by Echopixel | Echopixel | Device Malfunction | Nationwide |
| Device | CLASS II | Upgrade to MR recalled by Philips North America | Philips North America | Other | Nationwide |
| Device | CLASS II | Ingenia 1.5T recalled by Philips North America | Philips North America | Other | Nationwide |
| Device | CLASS II | Product Name: MR 5300; Model Numbers: (1) 782110, (2) recalled | Philips North America | Other | Nationwide |
| Device | CLASS I | Bard Blakemore Esophageal-Nasogastric Tube (Adult) recalled by C.R. Bard | C.R. Bard | Foreign Material | 44 states |
| Device | CLASS I | Bard Minnesota Four Lumen Esophagogastric Tamponade Tube recalled | C.R. Bard | Foreign Material | 44 states |
| Device | CLASS II | SmartPath to dStream for 1.5T recalled by Philips North America | Philips North America | Other | Nationwide |
| Device | CLASS II | BD Cathena Safety IV Catheter BD Multiguard Technology recalled | Becton Dickinson Infusion Therapy Systems | Packaging Defects | Nationwide |
| Device | CLASS II | SmartPath to dStream for XR and 3.0T recalled by Philips North America | Philips North America | Other | Nationwide |
| Device | CLASS II | Evolution Upgrade 1.5T recalled by Philips North America | Philips North America | Other | Nationwide |
| Device | CLASS I | Bard¿ Blakemore Esophageal-Nasogastric Tube (Child) recalled | C.R. Bard | Foreign Material | 44 states |
| Device | CLASS I | Endopath Echelon Vascular White Reload recalled by Ethicon Endo-Surgery | Ethicon Endo-Surgery | Other | Nationwide |
| Device | CLASS II | Ingenia Ambition recalled by Philips North America | Philips North America | Other | Nationwide |
| Device | CLASS I | Baxter Novum IQ Lvp Infusion System recalled by Baxter Healthcare | Baxter Healthcare | Other | IL |
| Device | CLASS II | SmartPath to Ingenia Elition recalled by Philips North America | Philips North America | Other | Nationwide |
| Device | CLASS II | Ingenia Elition recalled by Philips North America | Philips North America | Other | Nationwide |
| Device | CLASS II | Ingenia Ambition recalled by Philips North America | Philips North America | Other | Nationwide |
| Device | CLASS II | SmartPath to dStream for 3.0T recalled by Philips North America | Philips North America | Other | Nationwide |
| Device | CLASS II | Ingenia 1.5T recalled by Philips North America | Philips North America | Other | Nationwide |
| Device | CLASS II | Ingenia 3.0T recalled by Philips North America | Philips North America | Other | Nationwide |
| Device | CLASS II | Ingenia Elition recalled by Philips North America | Philips North America | Other | Nationwide |
| Device | CLASS II | PhenoMATRIX recalled by Copan WASP | Copan Wasp | Labeling Errors | Nationwide |
| Device | CLASS II | Meta-tan Lag/compression Screw Kit recalled by Smith & Nephew | Smith & Nephew | Other | Nationwide |
| Device | CLASS I | Bard¿ Blakemore Esophageal-Nasogastric Tube (Intermediate) recalled | C.R. Bard | Foreign Material | 44 states |
| Device | CLASS II | HiResolution" Bionic Ear System - M Battery Charger recalled | Advanced Bionics | Packaging Defects | 6 states |
| Device | CLASS II | Check=Flo Performer Introducer, 14., Reference recalled | Cook | Other | Nationwide |
| Device | CLASS II | Product Name: MR 7700; Model Numbers: (1) 782120, (2) recalled | Philips North America | Other | Nationwide |
| Device | CLASS II | Ingenia 1.5T CX recalled by Philips North America | Philips North America | Other | Nationwide |
| Device | CLASS I | IOPS Guidewire recalled by Centerline Biomedical | Centerline Biomedical | Device Malfunction | 8 states |
| Device | CLASS II | Ingenia 3.0T CX recalled by Philips North America | Philips North America | Other | Nationwide |
| Device | CLASS II | Check=Flo Performer Introducer, 10., Reference recalled | Cook | Other | Nationwide |
| Device | CLASS II | Evolution Upgrade 3.0T recalled by Philips North America | Philips North America | Other | Nationwide |
| Device | CLASS II | True 3d Viewer System recalled by Echopixel | Echopixel | Labeling Errors | Nationwide |
| Device | CLASS I | Bard¿ Single Intragastric Linton Balloon Tube recalled by C.R. Bard | C.R. Bard | Foreign Material | 44 states |
| Drug | CLASS II | Cura Hongos, Antifungal, 1% Clotrimazole, Topical Lotion recalled | Kenil Healthcare Private | Manufacturing (CGMP) Deviations | DE, NC |
| Drug | CLASS II | BD ChloraPrep Clear, 2% x/v chlorhexidine gluconate recalledChloraprep One-step | CareFusion 213 | Sterility | Nationwide |
| Drug | CLASS II | Cinnafresh anticavity gel toothpaste, sodium fluoride recalled | Kenil Healthcare Private | Manufacturing (CGMP) Deviations | DE, NC |
| Drug | CLASS II | Kofal, Athletes, Penetrating Pain Relief recalledKofal | Kenil Healthcare Private | Manufacturing (CGMP) Deviations | DE, NC |
| Drug | CLASS II | Rapidol, Triple Antibiotic First Aid Ointment recalledRapidol | Kenil Healthcare Private | Manufacturing (CGMP) Deviations | DE, NC |
| Drug | CLASS II | Kofal Original, Penetrating Pain Relieving Ointment recalled | Kenil Healthcare Private | Manufacturing (CGMP) Deviations | DE, NC |
| Drug | CLASS II | Cura Hongos, Antifungal Cream, Clotrimazole recalled | Kenil Healthcare Private | Manufacturing (CGMP) Deviations | DE, NC |
| Drug | CLASS II | Phentermine Hydrochloride Capsules, USP 30mg recalled by KVK TechPhentermine Hydrochloride | KVK Tech | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Nature Mint, Anticavity Fluoride Toothpaste recalled | Kenil Healthcare Private | Manufacturing (CGMP) Deviations | DE, NC |
| Drug | CLASS II | Nature Mint, Anticavity Fluoride Toothpaste recalled | Kenil Healthcare Private | Manufacturing (CGMP) Deviations | DE, NC |
| Drug | CLASS II | Maximum Security, Anticavity Gel Toothpaste recalled | Kenil Healthcare Private | Manufacturing (CGMP) Deviations | DE, NC |
| Drug | CLASS II | Esomeprazole Magnesium for Delayed-Release Oral Suspension recalledEsomeprazole Magnesium | Zydus Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS II | Maximum Security, Anticavity Gel Toothpaste recalled | Kenil Healthcare Private | Manufacturing (CGMP) Deviations | DE, NC |
| Drug | CLASS II | Indomethacin Extended-Release Capsules USP, 75 mg recalled by KVK TechIndomethacin | KVK Tech | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Nature Mint, Anticavity Fluoride Toothpaste recalled | Kenil Healthcare Private | Manufacturing (CGMP) Deviations | DE, NC |
| Drug | CLASS II | Kingskin, SacaCallos, 17% Salicylic acid recalled | Kenil Healthcare Private | Manufacturing (CGMP) Deviations | DE, NC |
| Drug | CLASS II | Rapidol Maximum Strength, Hydrocortisone 1% Anti-Itch Cream recalledRapidol | Kenil Healthcare Private | Manufacturing (CGMP) Deviations | DE, NC |
| Drug | CLASS II | Artridon Glucosamine (menthol 2% and Methyl Salicylate recalledArtridon | Kenil Healthcare Private | Manufacturing (CGMP) Deviations | DE, NC |
| Drug | CLASS II | Optim V, Anti-Itch Cream, Benzocaine 20% & Resorcinol recalled | Kenil Healthcare Private | Manufacturing (CGMP) Deviations | DE, NC |
| Drug | CLASS II | Maximum Security Anticavity Gel Toothpaste recalled | Kenil Healthcare Private | Manufacturing (CGMP) Deviations | DE, NC |
| Drug | CLASS II | Esomeprazole Magnesium for Delayed-Release Oral Suspension recalledEsomeprazole Magnesium | Zydus Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS II | Maximum Security, Anticavity Gel Toothpaste recalled | Kenil Healthcare Private | Manufacturing (CGMP) Deviations | DE, NC |
| Drug | CLASS II | Nature Mint, Anticavity Fluoride Toothpaste recalled | Kenil Healthcare Private | Manufacturing (CGMP) Deviations | DE, NC |
| Drug | CLASS II | Nature Mint Anticavity Fluoride Toothpaste recalled | Kenil Healthcare Private | Manufacturing (CGMP) Deviations | DE, NC |
| Drug | CLASS II | Airsupra (albuterol and budesonide) inhalation aerosol recalledAirsupra | AsttraZeneca Pharmaceuticals | Packaging Defects | Nationwide |
| Drug | CLASS II | Nature Mint Anticavity Fluoride Toothpaste recalled | Kenil Healthcare Private | Manufacturing (CGMP) Deviations | DE, NC |
| Food | CLASS I | Canned Beef Stew Product recalled by Hormel Foods | Hormel Foods | Foreign Material | |
| Food | CLASS II | Traditional Salsa is refrigerated product recalled by Frobright SalsaryTraditional | Frobright Salsary | Particulate Matter | 4 states |
| Food | CLASS I | Organic traditions Jumbo Pumpkin Seeds;;; Packaged recalledtraditions | Advantage Health Matters | Salmonella | NJ, NY, VA |
| Food | CLASS II | Mild Salsa is refrigerated product recalled by Frobright Salsary | Frobright Salsary | Particulate Matter | 4 states |
| Food | CLASS II | Medium Salsa Costco recalled by Frobright Salsary | Frobright Salsary | Particulate Matter | 4 states |
| Food | CLASS II | Mens Room Roasted Red Salsa is refrigerated product recalledMens Room | Frobright Salsary | Particulate Matter | 4 states |
| Food | CLASS I | Yellowstone Brown Sugar Molasses Baked Beans recalledYellowstone Brown | Vietti Acquisitions | Undeclared Soy | 23 states |
| Food | CLASS II | Medium Salsa is refrigerated product recalled by Frobright Salsary | Frobright Salsary | Particulate Matter | 4 states |
| Food | CLASS I | Lactoferrin as Apolactoferrin, 300 mg per serving recalled by My LifeLactoferrin | My Life | Undeclared Milk | Nationwide |
| Food | CLASS I | Zeke's Daddy's Granola recalled by BBF MassachusettsZeke's Daddy's | BBF Massachusetts | Undeclared Tree Nuts | NJ |
| Food | CLASS II | Pineapple Mango Salsa is refrigerated product recalled | Frobright Salsary | Particulate Matter | 4 states |
| Food | CLASS II | Hot Salsa is refrigerated product recalled by Frobright Salsary | Frobright Salsary | Particulate Matter | 4 states |
| Food | CLASS I | Enoki Mushroom in a, green marked recalled by Harvest NycEnoki | Harvest Nyc | Listeria | CT, NY, VT |
| Food | CLASS II | Verde Salsa is refrigerated product recalled by Frobright SalsaryVerde | Frobright Salsary | Particulate Matter | 4 states |
| Food | HEALTH ALERT | Chicken Soup Product recalled by FSIS | FSIS | Undeclared Wheat & Gluten | |
| Device | CLASS II | Centurion Sterile Weitlaner Retractor recalled by MEDLINE INDUSTRIES, LP | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | Pruitt Irrigation Occlusion Catheter recalled by LeMaitre Vascular | LeMaitre Vascular | Sterility | Nationwide |
| Device | CLASS I | AirLife Infant Heated Wire Circuit recalled by Vyaire Medical | Vyaire Medical | Device Malfunction | Nationwide |
| Device | CLASS I | Welch Allyn Life2000 Ventilation system recalled by Baxter Healthcare | Baxter Healthcare | Other | IL |
| Device | CLASS II | KliniTray. KlinioTray. Tissue resection margin examination recalled | Klinika Mdical Gmb | Sterility | Nationwide |
| Device | CLASS II | Perc Pin Adaptor recalled by Augmedics | Augmedics | Other | Nationwide |
| Device | CLASS II | Intera CV recalled by Philips Medical Systems | Philips Medical Systems Nederl | Packaging Defects | Nationwide |
| Device | CLASS I | MedicaLyte Liquid Bicarbonate Concentrate recalled | Nipro Renal Soultions USA | Foreign Material | Nationwide |
| Device | CLASS II | TufTex Over-the-Wire Embolectomy Catheter recalled by LeMaitre Vascular | LeMaitre Vascular | Sterility | Nationwide |
| Device | CLASS II | Pruitt Occlusion Catheter recalled by LeMaitre Vascular | LeMaitre Vascular | Sterility | Nationwide |
| Device | CLASS II | Halyard Suture Pack Cabg recalled by AVID Medical | Avid Medical | Other | Nationwide |
| Device | CLASS II | Contour Gold Eyelid Weight recalled by Meddev | Meddev | Labeling Errors | Nationwide |
| Device | CLASS II | Intera 1.0T Power/Pulsar recalled by Philips Medical Systems | Philips Medical Systems Nederl | Packaging Defects | Nationwide |
| Device | CLASS II | Intera 1.5T recalled by Philips Medical Systems | Philips Medical Systems Nederl | Packaging Defects | Nationwide |
| Device | CLASS II | LifeShield Drug Library Management (DLM), LifeShield Infusion Safety recalled | ICU Medical | Device Malfunction | Nationwide |
| Device | CLASS II | Intera 1.5T R11 recalled by Philips Medical Systems | Philips Medical Systems Nederl | Packaging Defects | Nationwide |
| Device | CLASS I | iGo¿2 DC Car Adapter to be used recalled by Medical Depot | Medical Depot | Foreign Material | Nationwide |
| Device | CLASS II | Intera 1.5T Power/Pulsar recalled by Philips Medical Systems | Philips Medical Systems Nederl | Packaging Defects | Nationwide |
| Device | CLASS II | Intera 3.0T Quasar Dual recalled by Philips Medical Systems | Philips Medical Systems Nederl | Packaging Defects | Nationwide |
| Device | CLASS I | Welch Allyn Life2000 Compressor recalled by Baxter Healthcare | Baxter Healthcare | Other | IL |
| Device | CLASS II | Contour Gold Eyelid Weight recalled by Meddev | Meddev | Labeling Errors | Nationwide |
| Device | CLASS II | KliniTray Platte Faxitron ,groB "R" sterile recalled | Klinika Mdical Gmb | Sterility | Nationwide |
| Device | CLASS II | Intera 0.5T Standard recalled by Philips Medical Systems | Philips Medical Systems Nederl | Packaging Defects | Nationwide |
| Device | CLASS II | Intera 1.5T Omni/Stellar recalled by Philips Medical Systems | Philips Medical Systems Nederl | Packaging Defects | Nationwide |
| Device | CLASS II | Alinity m Resp-4-Plex Amplification (AMP) Kit (CE) recalled | Abbott Molecular | Other | Nationwide |
| Device | CLASS I | AirLife Infant Heated Wire Circuit recalled by Vyaire Medical | Vyaire Medical | Device Malfunction | Nationwide |
| Device | CLASS II | PiezoWave 2 Control Unit, Product Number 100506US recalled | Richard Wolf | Device Malfunction | GA |
| Device | CLASS II | Enterprise 1.5T recalled by Philips Medical Systems | Philips Medical Systems Nederl | Packaging Defects | Nationwide |
| Device | CLASS II | Halyard Rapides E-pack recalled by AVID Medical | Avid Medical | Other | Nationwide |
| Device | CLASS II | Intera 1.0T Omni/Stellar recalled by Philips Medical Systems | Philips Medical Systems Nederl | Packaging Defects | Nationwide |
| Device | CLASS II | Tornado Embolization Microcoil, intended recalled by Cook Incorporated | Cook | Other | IN |
| Device | CLASS II | Alinity m Resp-4-Plex AMP Kit, List Number 09N79 recalled | Abbott Molecular | Other | Nationwide |
| Device | CLASS II | Halyard Christ Suture Kit recalled by AVID Medical | Avid Medical | Other | Nationwide |
| Device | CLASS II | SmartPath to dStream for 1.5T recalled by Philips Medical Systems | Philips Medical Systems Nederl | Packaging Defects | Nationwide |
| Device | CLASS II | FoundationOne Companion Diagnostic (F1CDx) recalled | Foundation Medicine | Other | Nationwide |
| Device | CLASS II | DxC 500 AU Clinical Chemistry Analyzer recalled by Beckman Coulter | Beckman Coulter | Potency & Assay | 17 states |
| Device | CLASS II | Centurion Sterile Weitlaner Retractor Prong recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | Intera 1.5T Explorer/Nova Dual recalled by Philips Medical Systems | Philips Medical Systems Nederl | Packaging Defects | Nationwide |
| Device | CLASS II | SmartPath to dStream for 3.0T recalled by Philips Medical Systems | Philips Medical Systems Nederl | Packaging Defects | Nationwide |
| Device | CLASS II | BIB Balloon in Balloon Dilatation Catheter recalled by Numed | Numed | Other | PA |
| Device | CLASS II | Intera 1.5T Master/Nova recalled by Philips Medical Systems | Philips Medical Systems Nederl | Packaging Defects | Nationwide |
| Drug | CLASS II | Testosterone Cypionate Injection, 200 mg/mL, CIII recalled | Empower Clinic Services | Sterility | Nationwide |
| Drug | CLASS II | La Roche-Posay Laboratoire Dermatologique Effaclar Duo Dual recalled | L'Oreal USA | Benzene | Nationwide |
| Drug | CLASS II | La Roche-Posay Laboratoire Dermatologique Effaclar recalled by L'Oreal U | L'Oreal USA | Benzene | Nationwide |
| Drug | CLASS II | La Roche-Posay Laboratoire Dermatologique Effaclar Duo Dual recalled | L'Oreal USA | Benzene | Nationwide |
| Food | CLASS I | Bonya Strawberry-Banana Yogurt Parfait recalled by KnockroeBonya Strawberry-Banana | Knockroe | Undeclared Tree Nuts | 4 states |
| Food | CLASS II | BIPC Flavored Ice Cream, Wells Enterprises recalledBipc Flavored | Wells Enterprises | Foreign Material | Nationwide |
| Food | CLASS II | Dixit Foods, Sabudana Khichadi recalled by BondsforeverDixit | Bondsforever | Undeclared Allergens | CA, UT, WA |
| Food | CLASS II | President Kumquat Slices recalled by East CK TradingPresident | East CK Trading | Undeclared Sulfites | 4 states |
| Food | CLASS II | Planet Smoothie ZSA Vanilla Flavored Fat Free Frozen Yogurt recalledPlanet Smoothie | Wells Enterprises | Foreign Material | Nationwide |
| Food | CLASS II | Ellington Farms Vanilla Flavored Ice Cream recalled by Wells EnterprisesEllington | Wells Enterprises | Foreign Material | Nationwide |
| Food | CLASS II | Artificially Flavored French Vanilla Ice Cream recalledArtificially Flavored | Wells Enterprises | Foreign Material | Nationwide |
| Food | CLASS II | Beijing Soybean Paste recalled by May Flower InternationalBeijing Soybean | May Flower International | Undeclared Wheat & Gluten | 12 states |
| Food | CLASS II | Vanilla Flavored Ice Cream, Wells Enterprises recalled | Wells Enterprises | Foreign Material | Nationwide |
| Food | CLASS II | GFGB Vanilla Bean Flavored Ice Cream, Wells Enterprises recalledGfgb | Wells Enterprises | Foreign Material | Nationwide |
| Food | CLASS I | Bonya Vanilla Yogurt Parfait with plastic inserts recalled by KnockroeBonya | Knockroe | Undeclared Tree Nuts | 4 states |
| Food | CLASS II | National Kasundi Peeled Mango Pickle IN Oil recalledNational | Advance Food International | Lead & Heavy Metals | 6 states |
| Food | CLASS II | GFGB 12% Vanilla Flavored Ice Cream, Wells Enterprises recalledGfgb | Wells Enterprises | Foreign Material | Nationwide |
| Food | CLASS II | Glenview Farms Artificially Flavored French Vanilla Ice Cream recalledGlenview | Wells Enterprises | Foreign Material | Nationwide |
| Food | CLASS I | Bonya Mango Yogurt Parfait with plastic inserts recalled by KnockroeBonya | Knockroe | Undeclared Tree Nuts | 4 states |
| Food | CLASS I | Bonya Blueberry Yogurt Parfait with plastic inserts recalled by KnockroeBonya | Knockroe | Undeclared Tree Nuts | 4 states |
| Food | CLASS I | Bonya Strawberry Yogurt Parfait with plastic inserts recalledBonya | Knockroe | Undeclared Tree Nuts | 4 states |
| Food | CLASS I | Bonya Coconut Yogurt Parfait with plastic inserts recalled by KnockroeBonya | Knockroe | Undeclared Tree Nuts | 4 states |
| Food | CLASS II | Dixit Foods, Pohe recalled by BondsforeverDixit | Bondsforever | Undeclared Allergens | CA, UT, WA |
| Food | CLASS II | Peanut Butter 'N Fudge Ice Cream, Wells Enterprises recalled | Wells Enterprises | Foreign Material | Nationwide |
| Food | CLASS II | Vanilla Bean Ice Cream with Madagascar vanilla recalled | Wells Enterprises | Foreign Material | Nationwide |
| Food | CLASS I | Bonya Black Cherry Yogurt Parfait with plastic inserts recalledBonya | Knockroe | Undeclared Tree Nuts | 4 states |
| Food | CLASS II | Glenview Farms Vanilla Flavored Ice Cream recalled by Wells EnterprisesGlenview | Wells Enterprises | Foreign Material | Nationwide |
| Food | CLASS I | Bonya Pineapple Yogurt Parfait with plastic inserts recalled by KnockroeBonya | Knockroe | Undeclared Tree Nuts | 4 states |
| Food | CLASS II | Cotton Candy Flavored Ice Cream, Wells Enterprises recalledCotton | Wells Enterprises | Foreign Material | Nationwide |
| Food | CLASS II | Quick Blend Vanilla Flavored Ice Cream, Wells Enterprises recalledQuick Blend | Wells Enterprises | Foreign Material | Nationwide |
| Food | CLASS II | Rocky Road Flavored Ice Cream, Wells Enterprises recalledRocky Road | Wells Enterprises | Foreign Material | Nationwide |
| Food | CLASS I | Tomatoes, retail Vine Ripe Tomatoes recalled by Ray & MascariTomatoes | Ray & Mascari | Salmonella | 7 states |
| Food | CLASS II | Mocha Almond Fudge Ice Cream, Wells Enterprises recalledMocha | Wells Enterprises | Foreign Material | Nationwide |
| Food | CLASS II | Gordon Choice Vanilla Flavored Ice Cream recalled by Wells EnterprisesGordon Choice | Wells Enterprises | Foreign Material | Nationwide |
| Food | CLASS I | Bonya Lemon Yogurt Parfait with plastic inserts recalled by KnockroeBonya | Knockroe | Undeclared Tree Nuts | 4 states |
| Food | CLASS II | Johnny Rockets Vanilla Flavored Ice Cream recalled by Wells EnterprisesJohnny Rockets | Wells Enterprises | Foreign Material | Nationwide |
| Food | CLASS I | H&C Farms Raw Premium Tomatoes, Naturally Grown from Seed recalledH&c | Hanshaw & Capling Farms | Salmonella | 8 states |
| Food | CLASS II | Keith Valley Vanilla Flavored Ice Cream recalled by Wells EnterprisesKeith Valley | Wells Enterprises | Foreign Material | Nationwide |
| Food | CLASS II | Glenview Farms Chocolate Ice Cream recalled by Wells EnterprisesGlenview | Wells Enterprises | Foreign Material | Nationwide |
| Food | CLASS I | Bonya Passion Fruit Yogurt Parfait with plastic inserts recalledBonya Passion | Knockroe | Undeclared Tree Nuts | 4 states |
| Food | CLASS II | Country Rich Vanilla Ice Cream, Wells Enterprises recalledCountry Rich | Wells Enterprises | Foreign Material | Nationwide |
| Food | CLASS II | Vanilla Frozen Yogurt, Wells Enterprises recalled | Wells Enterprises | Foreign Material | Nationwide |
| Food | CLASS II | Scooper Hero Ice Cream, Wells Enterprises recalledScooper Hero | Wells Enterprises | Foreign Material | Nationwide |
| Food | CLASS II | Blueberry Lemon Scones, bulk recalled by The Hot Chocolatier - St. Elmo | The Hot Chocolatier - St. Elmo | Undeclared Allergens | TN |
| Food | CLASS I | Bonya Peach Yogurt Parfait with plastic inserts recalled by KnockroeBonya Peach | Knockroe | Undeclared Tree Nuts | 4 states |
| Food | CLASS I | Bonya Raspberry Yogurt Parfait with plastic inserts recalled by KnockroeBonya | Knockroe | Undeclared Tree Nuts | 4 states |
| Food | CLASS II | New England Village Snacks The 19th Hole Snack Mix recalledNew England | Better Business...Better Foods | Undeclared Tree Nuts | NY |
| Food | CLASS I | Ready-To-Eat Smoked Andouille Sausage Products recalled | Bourgeois Smokehouse | Listeria | |
| Food | CLASS I | Ready-To-Eat Chicken Coxinhas Products recalled by Snack Mania Brazilian | Snack Mania Brazilian Delights Corp | Foreign Material | |
| Food | CLASS I | Ready-To-Eat Meat Pie Products recalled by Fijian Import & Export | Fijian Import & Export | Foreign Material | |
| Device | CLASS II | GALT Centeze Catheter recalled by Galt Medical | Galt Medical | Sterility | Nationwide |
| Device | CLASS II | aScope" 5 Broncho HD 5.6/2.8 Sampler Set recalled by Ambu | Ambu | Labeling Errors | Nationwide |
| Device | CLASS I | Intraocular lens recalled by Bausch & Lomb Surgical | Bausch & Lomb Surgical | Other | Nationwide |
| Device | CLASS II | Introducer Kit- Coaxial Dilator recalled by Galt Medical | Galt Medical | Sterility | Nationwide |
| Device | CLASS I | Codman Disposable Perforator Cranial perforator recalled | Integra LifeSciences Corp. (NeuroSciences) | Other | Nationwide |
| Device | CLASS II | Introducer Needle recalled by Galt Medical | Galt Medical | Sterility | Nationwide |
| Device | CLASS II | Introducer Kit- Tearaway MicroSlide recalled by Galt Medical | Galt Medical | Sterility | Nationwide |
| Device | CLASS II | Washer Disinfector Aquadis recalled by Getinge Disinfection Ab | Getinge Disinfection Ab | Packaging Defects | Nationwide |
| Device | CLASS I | Intraocular Lens recalled by Bausch & Lomb Surgical | Bausch & Lomb Surgical | Other | Nationwide |
| Device | CLASS II | Blueprint Software, BPUE001. Intended for use by surgeons as a pre recalled | Tornier S.A.S | Device Malfunction | Nationwide |
| Device | CLASS II | Bio 1 Granules for Filling ¿¿) recalled by Science & Bio Materials | Science & BIO Materials | Other | Nationwide |
| Device | CLASS II | B Braun Interventional Elite HV Hemostasis Valve Introducer System recalled | Galt Medical | Sterility | Nationwide |
| Device | CLASS II | Washer Disinfector Aquadis recalled by Getinge Disinfection Ab | Getinge Disinfection Ab | Packaging Defects | Nationwide |
| Device | CLASS I | Cadd Solis Hspca Pump ***Updated 5/27/26*** Scope updated recalled | Smiths Medical ASD | Device Malfunction | Nationwide |
| Device | CLASS II | Meridian Bioscience ImmunoCard STAT! Crypto/Giardia Test Kits recalled | Medline Industries LP - Northfield | Temperature Abuse | Nationwide |
| Device | CLASS II | Artix MT Thrombectomy Device recalled by Inari Medical - Oak Canyon | Inari Medical - Oak Canyon | Other | Nationwide |
| Device | CLASS II | Inspira Air Balloon Dilation System Airway balloon dilation catheter recalled | Integra LifeSciences Corp. (NeuroSciences) | Packaging Defects | Nationwide |
| Device | CLASS I | Cadd-Solis Infusion Pump recalled by Smiths Medical ASD | Smiths Medical ASD | Other | Nationwide |
| Device | CLASS II | B Braun Interventional Coaxial Dilator recalled by Galt Medical | Galt Medical | Sterility | Nationwide |
| Device | CLASS I | CADD Solis VIP Ambulatory Infusion Pump recalled by Smiths Medical ASD | Smiths Medical ASD | Other | Nationwide |
| Device | CLASS I | Codman Craniotomy Kit, Disposable Perforator Cranio-blade recalled | Integra LifeSciences Corp. (NeuroSciences) | Other | Nationwide |
| Device | CLASS II | GALT Guidewire recalled by Galt Medical | Galt Medical | Sterility | Nationwide |
| Device | CLASS I | Cadd-Solis VIP Ambulatory Infusion Pump recalled by Smiths Medical ASD | Smiths Medical ASD | Device Malfunction | Nationwide |
| Device | CLASS II | Atalante X, Powered Exoskeleton recalled by Wandercraft Sas | Wandercraft SAS | Other | NY, PA |
| Device | CLASS II | Philips Tempus Pro Patient Monitor recalled | Remote Diagnostic Technologies | Labeling Errors | Nationwide |
| Device | CLASS II | IntelliSpace Cardiovascular recalled by Philips Medical Systems | Philips Medical Systems Nederl | Device Malfunction | Nationwide |
| Device | CLASS I | Cadd-Solis Hpca Ambulatory Infusion Pump recalled by Smiths Medical ASD | Smiths Medical ASD | Device Malfunction | Nationwide |
| Device | CLASS II | Microstream Advance Neonatal-Infant Intubated CO2 Filter recalled | Philips North America | Other | Nationwide |
| Drug | CLASS II | Testosterone Pellet 200 mg (with Cholesterol </=2%) recalled by BSO | BSO | Particulate Matter | Nationwide |
| Drug | CLASS II | Carboxymethylcellulose Sodium Ophthalmic Solution recalledCarboxymethylcellulose Sodium | BRS Analytical Services | Sterility | Nationwide |
| Drug | CLASS II | Testosterone Pellet 200 mg Blunt (with Cholesterol </=2%) recalled | BSO | Particulate Matter | Nationwide |
| Drug | CLASS II | Lubricant Eye Drops Solution recalled by BRS Analytical ServicesLubricant Eye Drops Solution | BRS Analytical Services | Sterility | Nationwide |
| Drug | CLASS II | Testosterone Pellet 200 mg (with Cholesterol </=4%) recalled by BSO | BSO | Particulate Matter | Nationwide |
| Drug | CLASS II | Polyvinyl Alcohol Ophthalmic Solution recalledPolyvinyl Alcohol | BRS Analytical Services | Sterility | Nationwide |
| Drug | CLASS II | FentaNYL 500mcg (2mcg/mL) and Ropivacaine HCl 250mg recalled | Apollo Care | Sterility | MO |
| Drug | CLASS II | Testosterone Pellet 200 mg Blunt, 1 Pellet recalled by BSO | BSO | Particulate Matter | Nationwide |
| Drug | CLASS II | Carboxymethylcellulose Sodium Ophthalmic Gel recalled | BRS Analytical Services | Sterility | Nationwide |
| Drug | CLASS II | Testosterone Pellet 100 mg (with Cholesterol </=4%) recalled by BSO | BSO | Particulate Matter | Nationwide |
| Drug | CLASS I | Ropivacaine Hydrochloride Injection, USP, 0.5%, 500 mg per (5mg/mL) recalledRopivacaine Hydrochloride | Amneal Pharmaceuticals | Particulate Matter | Nationwide |
| Drug | CLASS II | Timolol Maleate Ophthalmic Solution USP, 0.5%, Sterile recalled by FDCTimolol Maleate | FDC | Other | Nationwide |
| Drug | CLASS II | Artificial Tears Ophthalmic Solution recalled by BRS Analytical ServicesArtificial Tears | BRS Analytical Services | Sterility | Nationwide |
| Drug | CLASS II | Clindamycin HCl Capsule, 300 mg, QTY recalled by RemedyRePack | RemedyRePack | Manufacturing (CGMP) Deviations | FL, PA, VA |
| Drug | CLASS II | temper tamer, 1 US fl oz., Homeopathic Oral Spray recalled | Siddha Flower Essences | Manufacturing (CGMP) Deviations | Nationwide |
| Food | CLASS I | Bone & Joint Restore recalled by Optimal CarnivoreBone | Optimal Carnivore | Salmonella | Nationwide |
| Food | CLASS II | Item M7204, frozen foodservice Lamb Weston Hashbrown Patties, frozen recalledItem M7204 | Lamb Weston | Foreign Material | AZ, HI |
| Food | CLASS II | Item M7414, frozen foodservice Lamb Weston Hashbrown Patties, frozen recalledItem M7414 | Lamb Weston | Foreign Material | AZ, HI |
| Food | CLASS II | Item M7422, frozen foodservice Lamb Weston Hashbrown Patties LW recalledItem M7422 | Lamb Weston | Foreign Material | AZ, HI |
| Food | CLASS I | Ankimo branded Monkfish Liver recalled by JJWV MarketingAnkimo | JJWV Marketing | Undeclared Allergens | CA |
| Food | CLASS I | Heinen's Honey Roasted Peanuts recalled by Trophy NutHeinen's | Trophy Nut | Labeling Errors | IL, OH |
| Food | CLASS II | Item M0053, frozen foodservice Lamb Weston Hashbrown Patties, frozen recalledItem M0053 | Lamb Weston | Foreign Material | AZ, HI |
| Food | CLASS I | Trader Joe's Sesame Miso Salad with Salmon recalledTrader Joe's | Taylor Farms Illinois | Undeclared Milk | 18 states |
| Food | HEALTH ALERT | Ready-To-Eat Chicken and Bacon Wrap Products recalled by FSIS | FSIS | Listeria | |
| Food | HEALTH ALERT | Ready-To-Eat Chicken and Bacon Wrap Products recalled | Rachael's Food | Listeria | |
| Device | CLASS II | epoc BGEM Crea Test Card for the epoc Blood Analysis System recalled | Siemens Healthcare Diagnostics | Device Malfunction | Nationwide |
| Device | CLASS II | IceSeed 1.5 CX Needle US, Cryoablation Needle recalled | Boston Scientific | Temperature Abuse | Nationwide |
| Device | CLASS II | Straight Inflow/Bifurcated Outflow Line Kit recalled | Belmont Instrument | Packaging Defects | Nationwide |
| Device | CLASS II | Medline procedure kits, labeled as: HAND recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS I | GE Healthcare Carestation 650c A1 recalled | GE Medical Systems China | Other | Nationwide |
| Device | CLASS II | Automated External Defibrillators recalled by Defibtech | Defibtech | Other | CT |
| Device | CLASS II | Medline procedure kits, labeled as: NON Sterile I&D KIT recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS I | GE Healthcare Carestation 750c A1 recalled | GE Medical Systems China | Other | Nationwide |
| Device | CLASS II | Medline procedure kits, labeled as: Wound Care Tray recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS I | GE Healthcare Carestation 620 A1 recalled by GE Medical Systems China Co | GE Medical Systems China | Other | Nationwide |
| Device | CLASS II | HistoCore Peloris recalled by Leica Biosystems Melbourne Pty | Leica Biosystems Melbourne | Packaging Defects | 14 states |
| Device | CLASS II | L-Shaped Femoral Augment recalled by Waldemar Link GmbH & Co. KG | Waldemar Link GmbH & Co. KG (Mfg Site) | Other | Nationwide |
| Device | CLASS II | Medline procedure kits, labeled as: Plastics Suture Tray recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | Quantum Informatics - Vision / Live Vue Monitor recalled | Spectrum Medical | Device Malfunction | 38 states |
| Device | CLASS II | Straight Inflow/Outflow Patient Line Kit recalled by Belmont Instrument | Belmont Instrument | Packaging Defects | Nationwide |
| Device | CLASS II | The Trimble RTS873 robotic total station is a solution recalled | Trimble Ab | Other | |
| Device | CLASS II | Medline procedure kits, labeled as: OL Ocular recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | Automated External Defibrillators recalled by Defibtech | Defibtech | Other | CT |
| Device | CLASS I | GE Healthcare Carestation 750 A1 recalled by GE Medical Systems China Co | GE Medical Systems China | Other | Nationwide |
| Device | CLASS II | Stratus CS Acute Care cTNI TestPak.IVD test recalled | Siemens Healthcare Diagnostics | Other | Nationwide |
| Device | CLASS I | GE Healthcare Carestation 650 A1 recalled by GE Medical Systems China Co | GE Medical Systems China | Other | Nationwide |
| Device | CLASS I | GE Healthcare Carestation 650 A1 recalled by GE Medical Systems China Co | GE Medical Systems China | Other | Nationwide |
| Device | CLASS I | GE Healthcare Carestation 750c A2 recalled | GE Medical Systems China | Other | Nationwide |
| Device | CLASS II | Distal Femoral Augment recalled by Waldemar Link GmbH & Co. KG | Waldemar Link GmbH & Co. KG (Mfg Site) | Other | Nationwide |
| Device | CLASS II | Automated External Defibrillators recalled by Defibtech | Defibtech | Other | CT |
| Device | CLASS II | Enhanced Verify Evaluation Handset (CFN HH90130FA) recalled | Medtronic Neuromodulation | Device Malfunction | Nationwide |
| Device | CLASS II | Hyperthermia Pump Procedure Kit recalled by Belmont Instrument | Belmont Instrument | Packaging Defects | Nationwide |
| Device | CLASS II | IceSeed 1.5 CX S Needle US, Cryoablation Needle recalled | Boston Scientific | Temperature Abuse | Nationwide |
| Device | CLASS II | Powered Laser Surgical Instrument Soltive Pro SuperPulsed recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS II | epoc BGEM BUN Test Card for the epoc Blood Analysis System recalled | Siemens Healthcare Diagnostics | Device Malfunction | Nationwide |
| Device | CLASS II | Quantum Informatics - Viper Monitor, Physiological, Patient recalled | Spectrum Medical | Device Malfunction | 38 states |
| Device | CLASS I | GE Healthcare Carestation 620 SE recalled by GE Medical Systems China Co | GE Medical Systems China | Other | Nationwide |
| Device | CLASS II | Automated External Defibrillators recalled by Defibtech | Defibtech | Other | CT |
| Device | CLASS I | GE Healthcare Carestation 650C A2 recalled | GE Medical Systems China | Other | Nationwide |
| Device | CLASS I | GE Healthcare Carestation 650 A2 recalled by GE Medical Systems China Co | GE Medical Systems China | Other | Nationwide |
| Device | CLASS I | GE Healthcare Carestation 620 A1 recalled by GE Medical Systems China Co | GE Medical Systems China | Other | Nationwide |
| Device | CLASS II | Medline procedure kits, labeled as: Reddy Joint Bath recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | IceSeed 1.5 CX Needle OUS, Cryoablation Needle recalled | Boston Scientific | Temperature Abuse | Nationwide |
| Device | CLASS II | Medline Sterile Water recalled by MEDLINE INDUSTRIES, LP | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS I | GE Healthcare Carestation 650 SE recalled by GE Medical Systems China Co | GE Medical Systems China | Other | Nationwide |
| Device | CLASS II | Medline Sterile 0.9% Normal Saline recalled by MEDLINE INDUSTRIES, LP | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | Medline procedure kits, labeled as: Sterile Prep Kit recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | Medline procedure kits, labeled as: T AND A PACK -LF recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | DxC 500 AU Clinical Chemistry Analyzer recalled by Beckman Coulter | Beckman Coulter | Device Malfunction | Nationwide |
| Device | CLASS II | IceSeed 1.5 CX S Needle OUS, Cryoablation Needle recalled | Boston Scientific | Temperature Abuse | Nationwide |
| Device | CLASS I | GE Healthcare Carestation 750 A2 recalled by GE Medical Systems China Co | GE Medical Systems China | Other | Nationwide |
| Device | CLASS II | Semi-Automated External Defibrillators recalled by Defibtech | Defibtech | Other | CT |
| Device | CLASS II | Tibial Augment recalled by Waldemar Link GmbH & Co. KG | Waldemar Link GmbH & Co. KG (Mfg Site) | Other | Nationwide |
| Device | CLASS II | Posterior Femoral Augment recalled by Waldemar Link GmbH & Co. KG | Waldemar Link GmbH & Co. KG (Mfg Site) | Other | Nationwide |
| Device | CLASS II | myQA iON; Article Number: MQ10 recalled by IBA Dosimetry | IBA Dosimetry | Other | Nationwide |
| Device | CLASS II | Disposable Set (4 sets/case) recalled by Belmont Instrument | Belmont Instrument | Packaging Defects | Nationwide |
| Device | CLASS I | GE Healthcare Carestation 650C A1 recalled | GE Medical Systems China | Other | Nationwide |
| Device | CLASS I | GE Healthcare Carestation 620 A2 recalled by GE Medical Systems China Co | GE Medical Systems China | Other | Nationwide |
| Drug | CLASS II | Levothyroxine Sodium Tablets, USP, 25 mcg (0.025 mg) recalledLevothyroxine Sodium | Accord Healthcare | Potency & Assay | Nationwide |
| Drug | CLASS II | Medroxyprogesterone Acetate Injectable Suspension recalled | Mckesson Medical-Surgical Inc. Corporate Office | Potency & Assay | FL, MS |
| Drug | CLASS II | Levothyroxine Sodium Tablets, USP, 50 mcg (0.05 mg) recalledLevothyroxine Sodium | Accord Healthcare | Potency & Assay | Nationwide |
| Drug | CLASS II | Clindamycin Hydrochloride Capsules, USP, 300mg recalled | Preferred Pharmaceuticals | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | niCARdipine Hydrochloride Injection, USP, 25 mg recalledNicardipine Hydrochloride | American Regent | Sterility | Nationwide |
| Drug | CLASS II | Infuvite Adult, multiple vitamins injection, Baxter recalledInfuvite Adult | Mckesson Medical-Surgical Inc. Corporate Office | Potency & Assay | FL, MS |
| Drug | CLASS II | Levothyroxine Sodium Tablets, USP, 112 mcg (0.112 mg) recalledLevothyroxine Sodium | Accord Healthcare | Potency & Assay | Nationwide |
| Drug | CLASS II | Dexonto 0.4% (dexamethasone sodium phosphate) solution recalled | Nubratori | Other | CA, PA |
| Drug | CLASS II | Tirofiban Hydrochloride Injection 5 mg recalled by Eugia USTirofiban | Eugia US | Potency & Assay | Nationwide |
| Drug | CLASS II | niCARdipine Hydrochloride Injection, USP, 25 mg recalledNicardipine Hydrochloride | American Regent | Sterility | Nationwide |
| Drug | CLASS II | Tirofiban Hydrochloride Injection 12.5 mg recalled by Eugia USTirofiban | Eugia US | Potency & Assay | Nationwide |
| Drug | CLASS II | Wegovy (semaglutide) injection recalled by Cardinal Health | Cardinal Health | Temperature Abuse | NC, SC, VA |
| Drug | CLASS II | Levothyroxine Sodium Tablets, USP, 88 mcg (0.088 mg) recalledLevothyroxine Sodium | Accord Healthcare | Potency & Assay | Nationwide |
| Food | CLASS I | Caraluzzi's Italian Style Seafood Burgers recalledCaraluzzi's | Caraluzzi's Markets | Undeclared Egg | CT |
| Food | CLASS II | Outer carton labeled: "Cookie Butter Banana Pie" Inner recalledOuter | Dianne's Fine Desserts | Undeclared Allergens | 16 states |
| Food | CLASS II | Sundae Shoppe, Cookies and Cream Mochi Ice Cream inside recalledSundae Shoppe | Gordon Desserts | Undeclared Wheat & Gluten | 4 states |
| Food | CLASS II | La Victoria Cilantro Salsa recalled by MegaMex FoodsLa Victoria | MegaMex Foods | Foreign Material | 5 states |
| Food | CLASS II | Dinstuhl's Pecan Brittle recalled by Dinstuhl's Fine Candy CompanyDinstuhl's | Dinstuhl's Fine Candy Company | Undeclared Allergens | MO, MS |
| Food | CLASS II | Chile Verde Egg Bites recalled by Valley Fine Foods CoChile Verde | Valley Fine Foods Co | Foreign Material | TX |
| Food | CLASS II | Emily Kate's Gluten Free Carrot Cake recalledEmily Kate's | Emily Kate's Foods | Foreign Material | WI |
| Food | CLASS II | Whole Grain Multigrain (corrugated), CP12, Frozen recalled | Upper Crust Bakery | Foreign Material | 6 states |
| Food | CLASS II | Ancient Grains Hoagie Roll (corrugated), CP45, Frozen recalledAncient Grains | Upper Crust Bakery | Foreign Material | 6 states |
| Food | CLASS II | Dinstuhl's Peanut Brittle recalled by Dinstuhl's Fine Candy CompanyDinstuhl's | Dinstuhl's Fine Candy Company | Undeclared Allergens | MO, MS |
| Food | CLASS II | Dinstuhl's Cashew Crunch recalled by Dinstuhl's Fine Candy CompanyDinstuhl's | Dinstuhl's Fine Candy Company | Undeclared Allergens | MO, MS |
| Food | CLASS II | Multigrain Sourdough Freshly Backed recalled by Giant EagleMultigrain | Giant Eagle | Foreign Material | 5 states |
| Food | CLASS II | Multigrain Sourdough (corrugated), CP12, Frozen recalledMultigrain | Upper Crust Bakery | Foreign Material | 6 states |
| Food | CLASS II | Emily Kate's Gluten Free Vanilla Cake recalledEmily Kate's | Emily Kate's Foods | Foreign Material | WI |
| Food | CLASS I | Ready-to-Eat Prosciutto Products recalled by Ferrarini USA Inc | Ferrarini USA Inc | Foreign Material | |
| Food | HEALTH ALERT | Bismillah Halal Meats Ground Beef recalled by FSIS | FSIS | E. coli | |
| Food | HEALTH ALERT | Ineligible Pork Cracklings Products recalled by FSIS | FSIS | Foreign Material | |