| Food | CLASS II | Pecorino Toscano D.O.P. Stagionato cheese wheels recalledPecorino Toscano | Elegant Foods | Listeria | WI |
| Food | CLASS I | Broccoli Sprouts recalled by Evergreen Fresh SproutsBroccoli Sprouts | Evergreen Fresh Sprouts | Salmonella | WA |
| Food | CLASS II | So Delicious Dairy Free Salted Caramel Cluster Cashewmilk recalledSo Delicious | WWF Operating | Foreign Material | Nationwide |
| Food | CLASS II | Powdered Sugar recalled by United Sugar Producers andPowdered | United Sugar Producers and Refiners | Packaging Defects | 7 states |
| Food | CLASS II | Light Brown Sugar recalled by United Sugar Producers and | United Sugar Producers and Refiners | Packaging Defects | 7 states |
| Food | CLASS III | American Ginsengs recalled by Kwok Shing | Kwok Shing | Other | CA |
| Food | CLASS I | Lemon Alfredo Fettuccine recalled by Gias Food | Gias Food | Listeria | Nationwide |
| Food | CLASS I | Fromagerie Coop de Mean Cabricharme recalled by WFM PurchasingFromagerie Coop | WFM Purchasing | Undeclared Egg | 7 states |
| Device | CLASS II | Medline Convenience Kits: Major Pack recalled by Medline Industries | Medline Industries | Other | Nationwide |
| Device | CLASS II | Medline Convenience Kits: Peds Sinus Pack recalled by Medline Industries | Medline Industries | Other | Nationwide |
| Device | CLASS II | SmartPath to dStream for XR and 3.0T recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Achieva 1.5T, Achieva 1.5T Conversion recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Medline Convenience Kits: Mfc Craniotomy Pack recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | PRO+ 36" MRS Surface, mattress recalled by Baxter Healthcare | Baxter Healthcare | Packaging Defects | Nationwide |
| Device | CLASS II | Pro+ Mrs Surface For Versacare, mattress recalled by Baxter Healthcare | Baxter Healthcare | Packaging Defects | Nationwide |
| Device | CLASS II | Volara System Volara, HC, NA recalled by Baxter Healthcare | Baxter Healthcare | Device Malfunction | Nationwide |
| Device | CLASS II | Ingenia Ambition S and Ingenia Ambition recalled | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | HF2P0ST9 HomeFill Oxygen System HomeFill Cylinder M9 recalled | Ventec Life Systems | Other | Nationwide |
| Device | CLASS II | Medline convenience kits containing Healthmark Instrument recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Name (Model Number): 1. Intera 1.5T (781195), 2. Intera 1.5T recalled | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Halyard IV Start Kit Non-sterile recalled by Avid Medical | Avid Medical | Packaging Defects | Nationwide |
| Device | CLASS II | Medline Convenience Kits: Major Neuro Vch recalled by Medline Industries | Medline Industries | Other | Nationwide |
| Device | CLASS I | Inca (Infant Nasal Cannulae Assy) Infant Nasal CPAP, Complete Set recalled | CooperSurgical | Other | Nationwide |
| Device | CLASS II | Extended Polyaxial Head, Attached Gimbal recalled | Seaspine Orthopedics | Other | Nationwide |
| Device | CLASS II | Philips EPIQ Elite Diagnostic Ultrasound System recalled | Philips Ultrasound | Labeling Errors | Nationwide |
| Device | CLASS II | IQvitals Zone, automatically recalled by Midmark | Midmark | Labeling Errors | Nationwide |
| Device | CLASS II | Olympus BiCOAG Hemostasis Probe Fixed Pin Connector recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS II | Ingenia 3.0T and Ingenia 3.0T CX recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Presource Convenience Kits: KIT, Usgpiv recalled by Cardinal Health 200 | Cardinal Health 200 | Packaging Defects | Nationwide |
| Device | CLASS II | PowerLED 300 Concealed Lighting System recalled by Maquet SAS | Maquet SAS | Other | Nationwide |
| Device | CLASS II | Evolution upgrade 1.5T and Evolution upgrade 3.0T recalled | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | REF:HF2PC9 HomeFill Oxygen System, HomeFill Cylinder M9 recalled | Ventec Life Systems | Other | Nationwide |
| Device | CLASS II | Pearle Vision 1 day (somofilcon A) Contact Lens recalled by CooperVision | CooperVision | Other | Nationwide |
| Device | CLASS I | Imager II Angiographic Catheters M001314001 Imager recalled | Boston Scientific | Other | Nationwide |
| Device | CLASS II | Presource Convenience Kits: KIT, PRE OP recalled by Cardinal Health 200 | Cardinal Health 200 | Packaging Defects | Nationwide |
| Device | CLASS II | Olympus BiCOAG Hemostasis Probe Coaxial Connector recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS II | Halyard IV Start Kit Non-sterile recalled by Avid Medical | Avid Medical | Packaging Defects | Nationwide |
| Device | CLASS II | PRO+ 40" MRS Surface, mattress recalled by Baxter Healthcare | Baxter Healthcare | Packaging Defects | Nationwide |
| Device | CLASS II | Achieva XR recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | REF: 81-030415 Myocardial Probe Non-Pyrogenic , 400 Series recalled | DeRoyal Industries | Temperature Abuse | Nationwide |
| Device | CLASS I | Halyard IV Start Kit Non-sterile recalled by Avid Medical | Avid Medical | Other | Nationwide |
| Device | CLASS II | Trinity Non-Surgical Isolation Gown, AAMI PB70 Level 2, X-Large recalled | New York Embroidery Studio | Packaging Defects | Nationwide |
| Device | CLASS II | REF: HF2POSTD HomeFill Oxygen System HomeFill cylinder D with CGA870 recalled | Ventec Life Systems | Other | Nationwide |
| Device | CLASS II | GmbH Spectralis with Flex Module recalled by Heidelberg Engineering | Heidelberg Engineering | Potency & Assay | Nationwide |
| Device | CLASS II | Medline Convenience Kits: Anterior Spine Pack recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Olympus EZDilate Endoscopic Balloon Dilator Wired-guided recalled | Olympus Corporation of the Americas | Other | PA |
| Device | CLASS II | Ingenia 1.5T, Ingenia 1.5T CX and Ingenia 1.5T recalled | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Olympus BiCOAG Hemostasis Probe Coaxial Connector recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS II | Cardioroot Woven Collagen Coated Vascular Graft recalled | SAS Intervascular | Other | Nationwide |
| Device | CLASS II | MR 5300 Model Number (REF): 1. recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | MR 7700 and Upgrade to MR recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Vitek 2 Ast-N461 Test Kit, Gram Negative Susceptibility recalled | Biomerieux | Other | MO |
| Device | CLASS II | IQvitals Zone, automatically recalled by Midmark | Midmark | Labeling Errors | Nationwide |
| Device | CLASS II | nGenuity Patient Monitor with Capnography recalled | Criticare Technologies | Device Malfunction | Nationwide |
| Device | CLASS II | Ingenia Elition S and Ingenia Elition recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | CombiSet Hemodialysis Blood Tubing Set recalled | Fresenius Medical Care Renal Therapies Group | Other | Nationwide |
| Device | CLASS II | IQvitals Zone, automatically recalled by Midmark | Midmark | Labeling Errors | Nationwide |
| Device | CLASS I | Inca (Infant Nasal Cannulae Assy) Neonatal Nasal CPAP recalled | CooperSurgical | Other | Nationwide |
| Device | CLASS II | Automated Impella Controller (AIC) recalled by Abiomed | Abiomed | Potency & Assay | Nationwide |
| Device | CLASS II | Achieva 3.0T recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | IQvitals Zone, automatically recalled by Midmark | Midmark | Labeling Errors | Nationwide |
| Device | CLASS II | Medline convenience kits containing Healthmark Instrument recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Olympus BiCOAG Hemostasis Probe Fixed Pin Connector recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Drug | CLASS II | Menow Sunscreen Pressed Powder SPF35 PA+++, Net content recalled | Shantou Qiwei industrial | Manufacturing (CGMP) Deviations | CA |
| Drug | CLASS II | Reliable-1 Laboratories Lubricating Tears, Sterile recalledLubricating Tears | Sterling Pharmaceutical Services | Sterility | Nationwide |
| Drug | CLASS II | Clear Eyes Redness Relief, Lubricant/Redness Reliever Eye recalled | Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare | Sterility | Nationwide |
| Drug | CLASS II | Walgreens Lubricant Eye Drops recalled by Sterling PharmaceuticalWalgreens Lubricant Eye Drops | Sterling Pharmaceutical Services | Sterility | Nationwide |
| Drug | CLASS II | Major LubriFresh P.M. Nighttime Ointment recalled | Sterling Pharmaceutical Services | Sterility | Nationwide |
| Drug | CLASS III | Olanzapine Tablets, USP 5 mg recalled by Macleods PharmaceuticalsOlanzapine | Macleods Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS II | Exenatide Injection, USP, 250 mcg/mL per prefilled pen recalledExenatide | Amneal Pharmaceuticals of New York | Other | Nationwide |
| Drug | CLASS II | Walgreens Lubricant Eye Drops Total Twin Pack recalledWalgreens Lubricant Eye Drops | Sterling Pharmaceutical Services | Sterility | Nationwide |
| Drug | CLASS II | Reliable -1 Laboratories, Sodium Chloride Hypertonicity recalledSodium Chloride Hypertonicity Ophthalmic Solution, 5% | Sterling Pharmaceutical Services | Sterility | Nationwide |
| Drug | CLASS II | Lubricant Eye Drops-Cameron Pharmaceuticals recalled | Sterling Pharmaceutical Services | Sterility | Nationwide |
| Drug | CLASS II | AvKare Carboxymethylcellulose Sodium Ophthalmic Solution recalledCarboxymethylcellulose Sodium | Sterling Pharmaceutical Services | Sterility | Nationwide |
| Drug | CLASS II | Clear Eyes Redness Relief, Lubricant/Redness Reliever Eye recalled | Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare | Sterility | Nationwide |
| Drug | CLASS II | AvKare Carboxymethylcellulose Sodium Ophthalmic Solution recalledCarboxymethylcellulose Sodium | Sterling Pharmaceutical Services | Sterility | Nationwide |
| Drug | CLASS II | TRP The Relief Products* Gentle Eyes Lubricant Eye Drops recalledGentle Eyes Lubricant Eye Drops | Sterling Pharmaceutical Services | Sterility | Nationwide |
| Food | ANNOUNCED | Sierra Nevada Graziers Monterey Jack, Jalapeno Jack recalledSierra Nevada Graziers | Sierra Nevada Cheese | E. coli | Nationwide |
| Food | CLASS I | Raw, Frozen Pork Sausage Products recalled by Fontanini Foods | Fontanini Foods | Foreign Material | |
| Food | CLASS I | Ready-To-Eat Chicken Stew Products recalled by Sempio Food Services | Sempio Food Services | Processing Deviation | |
| Food | ANNOUNCED | Deano’s Pasta products recalledDeano’s Pasta | Deano’s Pasta | Undeclared Fish & Shellfish | MA |
| Food | CLASS I | and Calco branded Alfalfa Sprouts recalled by Everything Sprouts | Everything Sprouts | Salmonella | MN, WI |
| Food | CLASS I | Mango Pico De Gallo recalled by Taylor Fresh Foods | Taylor Fresh Foods | Salmonella | 27 states |
| Food | CLASS II | Mercer's brand 6 Ice Cream Sandwiches TO GO recalledMercer's | Quality Dairy Farms | Undeclared Peanuts | NY |
| Food | CLASS I | Rice & Bean Burrito recalled by Taylor Fresh Foods | Taylor Fresh Foods | Salmonella | 27 states |
| Food | CLASS I | Pico De Gallo recalled by Taylor Fresh FoodsPico De | Taylor Fresh Foods | Salmonella | 27 states |
| Food | CLASS I | Diced Jalapenos recalled by Taylor Fresh Foods | Taylor Fresh Foods | Salmonella | 27 states |
| Food | CLASS I | Pico De Gallo Mild recalled by Taylor Fresh FoodsPico De | Taylor Fresh Foods | Salmonella | 27 states |
| Food | CLASS I | Pepper-jalapeno-dc 1/4"-4/5# Pepper-jalapeno-dc 1/4"-1/5# recalledPepper-jalapeno-dc | NatureBest Pre-Cut & Produce | Salmonella | LA, TX |
| Food | CLASS I | Robust Radish Mix recalled by Everything SproutsRobust Radish | Everything Sprouts | Salmonella | MN, WI |
| Food | CLASS I | Salsa Roja Medium recalled by Taylor Fresh Foods | Taylor Fresh Foods | Salmonella | 27 states |
| Food | CLASS I | Spicy Roast Beef Sandwich (closed-face) recalled by Taylor Fresh Foods | Taylor Fresh Foods | Salmonella | 27 states |
| Food | CLASS I | Spicy Jalapeno Jarlsberg Dip recalled by Taylor Fresh Foods | Taylor Fresh Foods | Salmonella | 27 states |
| Food | CLASS I | Mon Sire Brie, soft-ripened French cheese recalled by OptimusMon Sire | Optimus | Listeria | FL |
| Food | CLASS I | Zesty Garlic Mix, containing Garlic, Onion and Alfalfa Sprouts recalledZesty Garlic | Everything Sprouts | Salmonella | MN, WI |
| Food | CLASS I | Fiesta Salad with Shrimp recalled by Taylor Fresh FoodsFiesta | Taylor Fresh Foods | Salmonella | 27 states |
| Food | CLASS I | Authentic Guacamole recalled by Taylor Fresh FoodsAuthentic | Taylor Fresh Foods | Salmonella | 27 states |
| Food | CLASS I | Fresh Pico Tray recalled by Taylor Fresh Foods | Taylor Fresh Foods | Salmonella | 27 states |
| Food | CLASS I | Pico De Gallo Hot recalled by Taylor Fresh FoodsPico De | Taylor Fresh Foods | Salmonella | 27 states |
| Food | CLASS I | Heb-pico-mango- Pico De Gallo-mango- Pico De Gallo-mango recalledHeb-pico-mango- Pico | NatureBest Pre-Cut & Produce | Salmonella | LA, TX |
| Food | CLASS II | Coconut Flakes 537 Atlas Ave, Madison, WI recalled by Elegant Foods | Elegant Foods | Undeclared Sulfites | WI |
| Food | CLASS I | Pico De Gallo Spicy recalled by Taylor Fresh FoodsPico De | Taylor Fresh Foods | Salmonella | 27 states |
| Food | CLASS I | Salsa Fresca Medium recalled by Taylor Fresh Foods | Taylor Fresh Foods | Salmonella | 27 states |
| Food | CLASS I | Pico De Gallo-mild- Pico De Gallo-mild- Pico De Gallo-4/5# recalledPico De | NatureBest Pre-Cut & Produce | Salmonella | LA, TX |
| Food | CLASS I | Hot Pico De Gallo recalled by Taylor Fresh Foods | Taylor Fresh Foods | Salmonella | 27 states |
| Food | CLASS II | Golden Raisins 537 Atlas Ave, Madison, WI recalled by Elegant Foods | Elegant Foods | Undeclared Sulfites | WI |
| Food | CLASS I | Mild Pico De Gallo recalled by Taylor Fresh Foods | Taylor Fresh Foods | Salmonella | 27 states |
| Food | CLASS I | Heb-guac Kit-mild recalled by NatureBest Pre-Cut & ProduceHeb-guac Kit-mild | NatureBest Pre-Cut & Produce | Salmonella | LA, TX |
| Food | CLASS I | Salsa Verde Mild recalled by Taylor Fresh Foods | Taylor Fresh Foods | Salmonella | 27 states |
| Food | CLASS I | SOUP MIX- Tray, PPS971 CLR PET 900/cs 32cs/pal, film-sealed recalled | NatureBest Pre-Cut & Produce | Salmonella | LA, TX |
| Food | CLASS I | NatureBest Mild Cheddar & Jalapeno Stuffed Mushrooms Heb SI recalledNatureBest | NatureBest Pre-Cut & Produce | Salmonella | LA, TX |
| Food | CLASS I | BH Bold Chef Salad Kit recalled by Taylor Fresh FoodsBH Bold | Taylor Fresh Foods | Salmonella | 27 states |
| Food | CLASS II | Carrot Cake, 9". Keep Refrigerated/Frozen recalled by Elegant Foods | Elegant Foods | Other | WI |
| Food | CLASS II | Pumpkin Spice No Bake Cookie recalled by Best Friends BakeryPumpkin | Best Friends Bakery | Other | 10 states |
| Food | CLASS II | Buckhead, Tuna cs cs, 3- cs , Styrofoam container, Keep Refrigerated recalledBuckhead | Buckhead Meat Company D.B.A. Trinity Seafood | Other | 5 states |
| Food | CLASS I | Spicy Pimento Cheese Dip recalled by Taylor Fresh Foods | Taylor Fresh Foods | Salmonella | 27 states |
| Food | CLASS I | Pico De Gallo recalled by Taylor Fresh FoodsPico De | Taylor Fresh Foods | Salmonella | 27 states |
| Food | CLASS I | Taco Dip. Ingredients: Refried Vegetarian Beans *** recalled | Taylor Fresh Foods | Salmonella | 27 states |
| Food | CLASS II | Martina Fresh Whole Mangoes recalled by Panorama Produce SalesMartina | Panorama Produce Sales | Salmonella | 4 states |
| Food | CLASS I | Spicy Guacamole recalled by Taylor Fresh Foods | Taylor Fresh Foods | Salmonella | 27 states |
| Food | CLASS I | Heb-pico-medium- Pico De Gallo-medium- Pico De Gallo-medium recalledHeb-pico-medium- Pico | NatureBest Pre-Cut & Produce | Salmonella | LA, TX |
| Food | CLASS I | Pineapple Mango Salsa Mild recalled by Taylor Fresh Foods | Taylor Fresh Foods | Salmonella | 27 states |
| Food | CLASS I | Pico De Gallo recalled by Taylor Fresh FoodsPico De | Taylor Fresh Foods | Salmonella | 27 states |
| Food | CLASS III | Hexing Haw Balls candy recalled by Tiffany FoodHexing Haw | Tiffany Food | Foreign Material | 15 states |
| Food | CLASS I | Pico De Gallo-hot- Heb-pico-hot recalled by NatureBest Pre-Cut & ProducePico De | NatureBest Pre-Cut & Produce | Salmonella | LA, TX |
| Food | CLASS I | Tomato Salsa Fresca recalled by Taylor Fresh Foods | Taylor Fresh Foods | Salmonella | 27 states |
| Food | CLASS I | Crunchy Protein Sprout Mix, containing Alfalfa Fenugreek recalledCrunchy | Everything Sprouts | Salmonella | MN, WI |
| Device | CLASS II | Convenience kits Cataract Pack DYNJ59881A recalled by Medline Industries | Medline Industries | Sterility | Nationwide |
| Device | CLASS I | DuoGlide Short-Term Straight Dialysis Catheter recalled | Bard Access Systems | Other | 50 states |
| Device | CLASS II | Percutaneous Insertion Kit (PIK), dilator set recalled | Maquet Cardiopulmonary | Sterility | Nationwide |
| Device | CLASS II | Blood Culture Collection Venipuncture Kit 20/Cs recalled | Medical Action Industries Inc. 306 | Sterility | Nationwide |
| Device | CLASS II | DASH Rapid PCR Instrument recalled by Nuclein | Nuclein | Device Malfunction | Nationwide |
| Device | CLASS II | REF:2B5LT Ethicon Endo-Surgery recalled by Stryker Sustainability | Stryker Sustainability Solutions | Device Malfunction | Nationwide |
| Device | CLASS II | CADD Yellow Medication Cassette Reservoir with NRFit connector US recalled | ICU Medical | Packaging Defects | Nationwide |
| Device | CLASS II | EWO_02513 (Catalog number 320122) For Investigational Use Only Nano recalled | embecta Medical II | Other | Nationwide |
| Device | CLASS II | Axle Pin Assy Large Elbow Cobalt Chrome recalled by Howmedica Osteonics | Howmedica Osteonics | Other | Nationwide |
| Device | CLASS II | Aisys, Datex-Ohmeda anesthesia system recalled | Datex-Ohmeda | Device Malfunction | Nationwide |
| Device | CLASS II | Kinos Axiom Total Ankle System with Axiom PSR, Flat-cut (Cut Guide) recalled | restor3d | Packaging Defects | Nationwide |
| Device | CLASS I | Haylard Continuous Nerve Block Tray kits recalled by Avid Medical | Avid Medical | Sterility | 4 states |
| Device | CLASS I | Medline Convenience Kits: Port Access Kit Univ OF Ala recalled | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Triathlon Hinge Insert Size 4 5612-p-411 Triathlon Hinge recalled | Howmedica Osteonics | Other | Nationwide |
| Device | CLASS II | Convenience kits Minor Pack DYNJ58421A Springhill Minor recalled | Medline Industries | Sterility | Nationwide |
| Device | CLASS I | StatStrip Glucose Hospital Meter System recalled by Nova Biomedical | Nova Biomedical | Device Malfunction | Nationwide |
| Device | CLASS II | Enterprise Archive V8 recalled by GE Healthcare | GE Healthcare | Device Malfunction | Nationwide |
| Device | CLASS II | Philips Patient Information Center iX recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | REF:B11LT Ethicon Endo-Surgery, Inc. Xcel Bladeless Trocar recalled | Stryker Sustainability Solutions | Device Malfunction | Nationwide |
| Device | CLASS II | Workflow Core Services V8, intended to provide set recalled | GE Healthcare | Other | Nationwide |
| Device | CLASS II | Scorpio Recessed Metal Backed Patella 3045 recalled | Howmedica Osteonics | Foreign Material | Nationwide |
| Device | CLASS I | BD Alaris Pump Infusion Sets 10561554* recalled by BD Switzerland Sarl | BD Switzerland Sarl | Other | Nationwide |
| Device | CLASS II | SunMed Tracheal Tube, Size recalled by Well Lead Medical | Well Lead Medical | Other | Nationwide |
| Device | CLASS II | GM Helix Implant recalled by Straumann USA | Straumann USA | Packaging Defects | Nationwide |
| Device | CLASS II | EWO_02512 (Catalog number 320550) For Investigational Use Only Nano recalled | embecta Medical II | Other | Nationwide |
| Device | CLASS II | Bearing And Axle Bushing Assy Std Elbow C-m113-1-301 Krh recalled | Howmedica Osteonics | Other | Nationwide |
| Device | CLASS I | StatStrip Glucose and B- Ketone meter recalled by Nova Biomedical | Nova Biomedical | Device Malfunction | Nationwide |
| Device | CLASS II | Core Services Hub V8, a set of backend services including recalled | GE Healthcare | Other | Nationwide |
| Device | CLASS I | Halyard IV Start Kit Non-sterile recalled by Avid Medical | Avid Medical | Other | Nationwide |
| Device | CLASS II | IV Sets with drip chambers recalled by ICU Medical | ICU Medical | Particulate Matter | Nationwide |
| Device | CLASS II | Scorpio + Mobile Bearing Pcs 78-5-0910 System One Bipolar recalled | Howmedica Osteonics | Other | Nationwide |
| Device | CLASS I | Power-Trialysis Short-Term Straight Dialysis Catheter recalled | Bard Access Systems | Other | 50 states |
| Device | CLASS I | Medline Convenience Kits recalled by Medline Industries | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Duracon XL Angled Tib Ins C-m064-1-300 Self-pressurizing recalled | Howmedica Osteonics | Other | Nationwide |
| Device | CLASS II | All Poly Constrained Insert 69-2854 Nrg Knee Cr recalled | Howmedica Osteonics | Other | Nationwide |
| Device | CLASS II | REF:B12LT Ethicon Endo-Surgery, Inc. Xcel Bladeless Trocar recalled | Stryker Sustainability Solutions | Device Malfunction | Nationwide |
| Device | CLASS II | SNOO Sleep Sack, X-Large recalled by Happiest Baby | Happiest Baby | Other | Nationwide |
| Device | CLASS II | Convenience kits Anesthesia Pain PK League DYNJ67925A recalled | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Veriqa RT MonteCarlo 3D v3 recalled by PTW Freiburg | PTW Freiburg | Device Malfunction | Nationwide |
| Device | CLASS II | NOxBOXi Nitric Oxide Delivery System recalled | Noxbox | Packaging Defects | Nationwide |
| Device | CLASS II | IV Sets with drip chambers recalled by ICU Medical | ICU Medical | Particulate Matter | Nationwide |
| Device | CLASS II | Convenience kits Myringotomy Pack-lf DYNJ59097A recalled | Medline Industries | Sterility | Nationwide |
| Device | CLASS I | Haylard Basic Biopsy Tray kits recalled by Avid Medical | Avid Medical | Sterility | 4 states |
| Device | CLASS II | Percutaneous Insertion Kit (PIK), Guidewire recalled | Maquet Cardiopulmonary | Sterility | Nationwide |
| Device | CLASS I | Impella Optical Controller, Automated Impella Controller recalled | Abiomed | Device Malfunction | Nationwide |
| Device | CLASS II | StoneSmart Connect Console Contents: Power Cord recalled | Boston Scientific | Other | Nationwide |
| Device | CLASS I | Medline Convenience Kits recalled by Medline Industries | Medline Industries | Sterility | Nationwide |
| Device | CLASS I | Medline Convenience Kits: Open Heart Adult recalled | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Centricity Enterprise Archive V2, V3, and V4 recalled by GE Healthcare | GE Healthcare | Device Malfunction | Nationwide |
| Device | CLASS II | IV Non-Dedicated Gravity Administration Sets with drip chambers recalled | ICU Medical | Foreign Material | Nationwide |
| Device | CLASS II | Trident 0¿ Poly Insert ID 620-00-28D Orthopaedic implant recalled | Howmedica Osteonics | Other | Nationwide |
| Device | CLASS II | Omnifit Series I Acet recalled by Howmedica Osteonics | Howmedica Osteonics | Other | Nationwide |
| Device | CLASS I | Medline Convenience Kits recalled by Medline Industries | Medline Industries | Sterility | Nationwide |
| Device | CLASS I | Impella Optical Controller with the below product recalled by Abiomed | Abiomed | Device Malfunction | Nationwide |
| Device | CLASS II | Percutaneous Insertion Kit (PIK), Guidewire recalled | Maquet Cardiopulmonary | Sterility | Nationwide |
| Device | CLASS II | Hemospray Endoscopic Hemostat recalled by Wilson-Cook Medical | Wilson-Cook Medical | Device Malfunction | Nationwide |
| Device | CLASS II | Medrad¿ Stellant Flex Syringe Kit used recalled by Bayer Medical Care | Bayer Medical Care | Sterility | Nationwide |
| Device | CLASS II | Pi-Cardia Inc. ShortCut REF: Z-a-20.003-US recalled | PI Cardia | Other | Nationwide |
| Device | CLASS II | Centricity PACS V2, V3, V4, V6, V7 recalled by GE Healthcare | GE Healthcare | Device Malfunction | Nationwide |
| Device | CLASS II | REF:B5LT Ethicon Endo-Surgery recalled by Stryker Sustainability | Stryker Sustainability Solutions | Device Malfunction | Nationwide |
| Device | CLASS II | Acetabular Cup Uhmwpe 61-3258 All Poly Constrained Insert recalled | Howmedica Osteonics | Other | Nationwide |
| Device | CLASS II | Abg I Acetabular Insert Hooded Id C-m079-2-801 Arc2f recalled | Howmedica Osteonics | Other | Nationwide |
| Device | CLASS II | Captus 4000e Thyroid Uptake System recalled | Mirion Technologies (Capintec) | Device Malfunction | Nationwide |
| Device | CLASS II | REF:B5ST Ethicon Endo-Surgery recalled by Stryker Sustainability | Stryker Sustainability Solutions | Device Malfunction | Nationwide |
| Device | CLASS II | Reign Medical Clench Staple System (Compression), Description recalled | F & A Foundation | Other | Nationwide |
| Device | CLASS II | Scorpio C-dome Patella 73-2710 73-2910 Scorpio U-dome recalled | Howmedica Osteonics | Other | Nationwide |
| Device | CLASS I | Medline Convenience Kits: Kit Anesthesia L&d A- Line Set recalled | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Philips PIC iX Essentials recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | IV Sets with drip chambers recalled by ICU Medical | ICU Medical | Particulate Matter | Nationwide |
| Device | CLASS II | Plum administration sets recalled by ICU Medical | ICU Medical | Particulate Matter | Nationwide |
| Device | CLASS I | StatStrip Glucose Hospital Meter System recalled by Nova Biomedical | Nova Biomedical | Device Malfunction | Nationwide |
| Device | CLASS I | StatStrip Glucose and B- Ketone meter recalled by Nova Biomedical | Nova Biomedical | Device Malfunction | Nationwide |
| Device | CLASS I | Haylard Univ Imaging Biopsy Trucustom kits recalled by Avid Medical | Avid Medical | Sterility | 4 states |
| Device | CLASS I | Automated Impella Controller (AIC) recalled by Abiomed | Abiomed | Device Malfunction | Nationwide |
| Device | CLASS II | Centricity PACS Server V7, intended recalled by GE Healthcare | GE Healthcare | Other | Nationwide |
| Device | CLASS II | SNOO Sleep Sack, X-Small recalled by Happiest Baby | Happiest Baby | Other | Nationwide |
| Device | CLASS II | IV Sets with drip chambers recalled by ICU Medical | ICU Medical | Particulate Matter | Nationwide |
| Device | CLASS II | Medline Convenience Kit: Open Heart A Pack recalled | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Oncology sets with drip chambers recalled by ICU Medical | ICU Medical | Foreign Material | Nationwide |
| Device | CLASS II | Aisys CS2, Datex-Ohmeda anesthesia system recalled | Datex-Ohmeda | Device Malfunction | Nationwide |
| Device | CLASS II | Oncology sets with drip chambers recalled by ICU Medical | ICU Medical | Foreign Material | Nationwide |
| Device | CLASS I | StatStrip Glucose and B- Ketone meter recalled by Nova Biomedical | Nova Biomedical | Device Malfunction | Nationwide |
| Device | CLASS II | Carescape Central Station CSCS V3 MAS800 Desktop recalled | GE Medical Systems Information Technologies | Device Malfunction | Nationwide |
| Device | CLASS I | Medline Convenience Kits recalled by Medline Industries | Medline Industries | Sterility | Nationwide |
| Device | CLASS I | Haylard Single Shot Epi Tray kits recalled by Avid Medical | Avid Medical | Sterility | 4 states |
| Device | CLASS II | Et Control recalled by Datex-Ohmeda | Datex-Ohmeda | Device Malfunction | Nationwide |
| Device | CLASS II | Aisys CS2 with Et Control, Datex-Ohmeda anesthesia system recalled | Datex-Ohmeda | Device Malfunction | Nationwide |
| Device | CLASS II | REF:2B5ST Ethicon Endo-Surgery recalled by Stryker Sustainability | Stryker Sustainability Solutions | Device Malfunction | Nationwide |
| Drug | CLASS II | Dopamine HCl Inj., USP, 200 mg/ (40 mg/mL) Single-dose recalledDopamine Hydrochloride | Pfizer | Sterility | Nationwide |
| Drug | CLASS II | Chlorthalidone Tablets, USP, 25 mg recalled by Inventia HealthcareChlorthalidone | Inventia Healthcare | Potency & Assay | Nationwide |
| Drug | CLASS II | Lidocaine Ointment USP, 5%, Speermint Flavor recalledLidocaine | SUN Pharma /Taro | Potency & Assay | Nationwide |
| Drug | CLASS II | Fluphenazine HCl Elixir, USP, 2.5 mg per, Delivers recalled | Safecor Health | Potency & Assay | Nationwide |
| Drug | CLASS II | Fluphenazine HCl Elixir, USP, 5 mg per, Delivers recalled | Safecor Health | Potency & Assay | Nationwide |
| Drug | CLASS II | Fluphenazine HCl Elixir, USP, 5 mg per, Delivers recalled | Safecor Health | Potency & Assay | Nationwide |
| Drug | CLASS I | Thyroid Tablets, USP, 1/2 Grain (30 mg) recalledThyroid | Vitruvias Therapeutics | Potency & Assay | Nationwide |
| Drug | CLASS II | Fluphenazine HCl Elixir, USP, 10 mg per, Delivers recalled | Safecor Health | Potency & Assay | Nationwide |
| Drug | CLASS II | Fluphenazine HCl Elixir, USP, 20 mg per, Delivers recalled | Safecor Health | Potency & Assay | Nationwide |
| Drug | CLASS II | Fluphenazine HCl Elixir, USP, 15 mg per, Delivers recalled | Safecor Health | Potency & Assay | Nationwide |
| Food | CLASS I | Organic Triple Berry Blend Strawberries, Blackberries & Blueberries recalled | Frutas y Hortalizas del Sur | E. coli | AR |
| Food | CLASS I | organic moringa leaf powder recalled by Foods Alive | Foods Alive | Salmonella | Nationwide |
| Food | CLASS I | Raw Pork, Beef, and Goat Products recalled by Star Meat Delivery | Star Meat Delivery | Undeclared Allergens | |
| Food | ANNOUNCED | Wholesome Pantry Organic Unsweetened Apple Sauce recalledWholesome Pantry | Wakefern Food | Foreign Material | |
| Food | ANNOUNCED | Niwali Tejocote Capsules and Pieces recalled by Global MixNiwali | Global Mix | Foreign Material | Nationwide |
| Drug | ANNOUNCED | ICU Medical LLC 0.9% Sodium Chloride Injection recalledICU Medical LLC | Otsuka ICU Medical | Packaging Defects | |
| Drug | ANNOUNCED | Par Pharmaceutical Dexmedetomidine HCl recalled by Par HealthPar Pharmaceutical | Par Health | Particulate Matter | Nationwide |
| Food | ANNOUNCED | J. Higgs Loaded Bacon & Cheddar Potato Chips recalledJ. HIGGS | Saratoga Potato Chips | Undeclared Soy | 5 states |
| Food | ANNOUNCED | Truly AIP, EAT G.A.N.G.S.T.E.R All purpose flour, bread mix recalledTruly AIP, EAT G.A.N.G.S.T.E.R | GF Blends | Undeclared Wheat & Gluten | Nationwide |
| Drug | CLASS II | fentaNYL Citrate, 1,000 mcg recalled by OurPharma | OurPharma | Other | Nationwide |
| Food | CLASS II | Fannie May & XO Marshmallow Pixie S'mores Collection recalledFannie May | Ferrero USA | Undeclared Tree Nuts | 4 states |
| Food | CLASS I | Alfalfa, Net Weight 50 lbs. bag, Product of USA, International recalledAlfalfa | International Sprout Holdings | Salmonella | 17 states |
| Food | CLASS I | Momchipz Gluten Free Veggie Chips Broccoli Florets & Cauliflower recalledMomchipz | Exotique Foods Canada | Undeclared Wheat & Gluten | |
| Food | CLASS II | Prolon Everyday Apulian Almond & Cocoa Spread recalled by L-NutraProlon Everyday | L-Nutra | Undeclared Allergens | Nationwide |
| Food | CLASS I | Crown Farms Dried Suri Cut, 200 gm per, keep frozen recalledCrown | Euro Foods Group USA NJ | Foreign Material | 4 states |
| Device | CLASS II | Getinge PVC Thoracic Catheter, Soft PVC Right Angle recalled | Atrium Medical | Potency & Assay | Nationwide |
| Device | CLASS II | Products that contain the Pericare Wipes: *Bardex¿ I.C recalled | C.R. Bard | Other | Nationwide |
| Device | CLASS I | Bravo CF capsule delivery device, Product Number FGS recalled | Given Imaging | Device Malfunction | Nationwide |
| Device | CLASS II | Citric Complete Dry Citric Acid Concentrate recalled | Nipro Renal Soultions USA | Other | Nationwide |
| Device | CLASS II | Products that contain the Pericare Wipes recalled by C.R. Bard | C.R. Bard | Other | Nationwide |
| Device | CLASS I | Kit: Epidural/Pain TQC 20/Cs recalled by Medical Action Industries | Medical Action Industries Inc. 306 | Sterility | 6 states |
| Device | CLASS II | Halyard IV Start Kit Non-Sterile recalled by Avid Medical | Avid Medical | Sterility | Nationwide |
| Device | CLASS I | Kit: Single Shot Epidural 20/Cs recalled by Medical Action Industries | Medical Action Industries Inc. 306 | Sterility | 6 states |
| Device | CLASS II | AMS Convenience Kit: Dsaek Pack - RX recalled | Windstone Medical Packaging | Device Malfunction | Nationwide |
| Device | CLASS II | MedicaLyte Bicarbonate Powder recalled by Nipro Renal Soultions USA | Nipro Renal Soultions USA | Other | Nationwide |
| Device | CLASS II | Products that contain the Pericare Wipes recalled by C.R. Bard | C.R. Bard | Other | Nationwide |
| Device | CLASS II | Citric Complete Liquid Citric Acid Concentrate recalled | Nipro Renal Soultions USA | Other | Nationwide |
| Device | CLASS II | Getinge PVC Thoracic Catheter, Firm PVC Straight recalled | Atrium Medical | Potency & Assay | Nationwide |
| Device | CLASS II | Products that contain the Pericare Wipes recalled by C.R. Bard | C.R. Bard | Temperature Abuse | Nationwide |
| Device | CLASS II | Products that contain the Pericare Wipes recalled by C.R. Bard | C.R. Bard | Temperature Abuse | Nationwide |
| Device | CLASS II | Getinge PVC Thoracic Catheter, Soft PVC Straight recalled | Atrium Medical | Potency & Assay | Nationwide |
| Device | CLASS II | Products that contain the Pericare Wipes recalled by C.R. Bard | C.R. Bard | Other | Nationwide |
| Device | CLASS II | DermaV Laser System recalled by Lutronic | Lutronic | Other | Nationwide |
| Device | CLASS II | MedicaLyte Liquid Bicarbonate Concentrate recalled | Nipro Renal Soultions USA | Other | Nationwide |
| Drug | CLASS I | Dextrose Injection, USP, 70 % recalled by Baxter Healthcare | Baxter Healthcare | Particulate Matter | Nationwide |
| Drug | CLASS III | Fluphenazine Hydrochloride Tablets, USP, 1mg recalledFluphenazine Hydrochloride | Ajanta Pharma USA | Potency & Assay | Nationwide |
| Drug | CLASS III | Povidone Iodine 1.25% / Proparacaine HCl 0.5% Ophthalmic recalled | ImprimisRx NJ | Potency & Assay | Nationwide |
| Drug | CLASS I | 0.9% Sodium Chloride Injection, USP Partial Fill recalledSodium Chloride | B Braun Medical | Particulate Matter | Nationwide |
| Drug | CLASS I | Epinephrine Injection, USP, 30 mg/ (1mg/mL)-Multiple-Dose Vial recalledEpinephrine | American Regent | Particulate Matter | Nationwide |
| Food | ANNOUNCED | biQ-FEL supplement recalled by A&P CreationsbiQ-FEL | A&P Creations | Hidden Drug Ingredients | |
| Food | ANNOUNCED | Bettergoods Italian Lemon Alfredo Fettuccine recalled by Gias FoodsBettergoods | Gias Foods | Listeria | Nationwide |
| Food | ANNOUNCED | So Delicious Dairy Free Salted Caramel Cluster Non-Dairy recalledSo Delicious Dairy Free | Danone USA | Foreign Material | |
| Drug | ANNOUNCED | Compounded Glutathione 200 mg/mL multidose vial recalledCentric Compounding | Centric Compounding | Packaging Defects | Nationwide |
| Food | ANNOUNCED | Whole Foods Market Cheese recalledWhole Foods Market | Whole Foods Market | Undeclared Egg | 7 states |
| Food | ANNOUNCED | No Brand Name Broccoli Sprouts recalled by Evergreen Fresh SproutsNo Brand Name | Evergreen Fresh Sprouts | Salmonella | ID, MT, WA |
| Drug | CLASS II | Prasugrel HCI, Tablets, USP, 10mg recalledPrasugrel | Golden State Medical Supply | Potency & Assay | Nationwide |
| Drug | CLASS II | Prasugrel Tablets, USP, 10mg recalled by Mylan PharmaceuticalsPrasugrel | Mylan Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS III | Revcovi (elapegademase-lvlr) Injection, 2.4mg/ (1.6 mg/mL) recalledRevcovi | Chiesi USA | Potency & Assay | MO, TN |
| Drug | CLASS II | 2% Chlorhexidine Gluconate* Cloth, Non-sterile recalled by Sage ProductsChlorhexidine Gluconate | Sage Products | Other | Nationwide |
| Drug | CLASS I | 0.9% Sodium Chloride Injection USP, Viaflex recalledSodium Chloride | Baxter Healthcare | Particulate Matter | IL |
| Drug | CLASS III | Buprenorphine Sublingual Tablets (C-iii), 2 mg recalledBuprenorphine | American Health Packaging | Packaging Defects | Nationwide |
| Drug | CLASS I | Glutathione 200 mg/mL sterile multidose vial recalled | Optimal Balance Pharmacy | Sterility | Nationwide |
| Device | CLASS II | Medline Convenience Kits: Blood Draw Kit recalled by Medline Industries | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Presource Packs Containing CliniClean Pericare Wipes within recalled | Cardinal Health 200 | Other | Nationwide |
| Device | CLASS II | Medline Convenience Kits containing BD ChloraPrep Clear recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | Medline Convenience Kits: Ortho Aspiration Kit recalled | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Neuro; Neuro; Crani; Ortho Spine Pack; Bmhm Neuro Pack recalled | Avid Medical | Sterility | Nationwide |
| Device | CLASS II | Presource Packs Containing CliniClean Pericare Wipes within recalled | Cardinal Health 200 | Other | Nationwide |
| Device | CLASS II | Presource Packs Containing CliniClean Pericare Wipes within recalled | Cardinal Health 200 | Other | Nationwide |
| Device | CLASS II | Lux-Dx, Lux-Dx II, Lux-Dx II+ Insertable Cardiac Monitor recalled | Boston Scientific | Device Malfunction | Nationwide |
| Device | CLASS II | Medline Convenience Kits containing BD ChloraPrep DYKA1054F recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | Lux-Dx, Lux-Dx II, Lux-Dx II+ Insertable Cardiac Monitor recalled | Boston Scientific | Device Malfunction | Nationwide |
| Device | CLASS II | Medline Convenience Kits: Arterial Line Insertion Kit recalled | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Medline Convenience Kits containing BD ChloraPrep Clear recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | Philips Brilliance recalled by Philips North America | Philips North America | Device Malfunction | MA |
| Device | CLASS II | Medline Convenience Kits: Colorectal ME recalled by Medline Industries | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Extension Set Discofix Four Way Stopcock recalled by B Braun Medical | B Braun Medical | Other | Nationwide |
| Device | CLASS II | 5008X HD/HDF with CLiC Blood Tubing Set recalled | Fresenius Medical Care Renal Therapies Group | Packaging Defects | Nationwide |
| Device | CLASS II | Medline Convenience Kits containing BD ChloraPrep Clear recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | Medline Convenience Kits containing BD ChloraPrep Clear recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | Presource Packs Containing CliniClean Pericare Wipes within recalled | Cardinal Health 200 | Other | Nationwide |
| Device | CLASS II | Medline Convenience Kits containing BD ChloraPrep Clear recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | Medline Convenience Kits: Pre-op KIT recalled by Medline Industries | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Medline Convenience Kits containing BD ChloraPrep-LF DYNJ42832B recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | Medline Convenience Kits containing BD ChloraPrep Clear recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | Medline Convenience Kits containing BD ChloraPrep Clear recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | Medline Convenience Kits: Drawer 9 Cricothyrotomy Kit recalled | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Medline Convenience Kits: Ivs Blood Culture Kit recalled | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Presource Packs Containing CliniClean Pericare Wipes within recalled | Cardinal Health 200 | Other | Nationwide |
| Device | CLASS II | Philips IQon Spectral CT recalled by Philips North America | Philips North America | Device Malfunction | MA |
| Device | CLASS II | Medline Convenience Kits recalled by Medline Industries | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Medline Convenience Kits: IV Start KIT recalled by Medline Industries | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Medline Convenience Kits: EYE KIT recalled by Medline Industries | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Presource Packs Containing CliniClean Pericare Wipes within recalled | Cardinal Health 200 | Foreign Material | Nationwide |
| Device | CLASS II | Medline Convenience Kits: IV Start Kit Lab Draw-sh recalled | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Medline Convenience Kits containing BD ChloraPrep Clear recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | 5008X HD/HDF Standard Blood Tubing Set recalled | Fresenius Medical Care Renal Therapies Group | Packaging Defects | Nationwide |
| Device | CLASS II | Medline Convenience Kits: C-section Prep recalled by Medline Industries | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Presource Packs Containing CliniClean Pericare Wipes within recalled | Cardinal Health 200 | Other | Nationwide |
| Device | CLASS II | Citrasate, Liquid Acid Concentrate recalled | Fresenius Medical Care Renal Therapies Group | Other | Nationwide |
| Device | CLASS II | Presource Packs Containing CliniClean Pericare Wipes within recalled | Cardinal Health 200 | Other | Nationwide |
| Device | CLASS II | NaturaLyte, Liquid Acid Concentrate recalled | Fresenius Medical Care Renal Therapies Group | Other | Nationwide |
| Device | CLASS II | Baxter Novum IQ Syringe Pump, Loaner recalled by Baxter Healthcare | Baxter Healthcare | Device Malfunction | Nationwide |
| Device | CLASS II | Medline Convenience Kits containing BD ChloraPrep Clear recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | Baxter Novum IQ Syringe Pump recalled by Baxter Healthcare | Baxter Healthcare | Device Malfunction | Nationwide |
| Device | CLASS II | Medline Convenience Kits: Labor CDS recalled by Medline Industries | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Medline Convenience Kits containing BD ChloraPrep Clear recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | Medline Convenience Kits: Ultrasound Breast Pack recalled | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Medline Convenience Kits recalled by Medline Industries | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Granuflo Dry Acid Concentrate: Product Numbers: 0FD2251-3B recalled | Fresenius Medical Care Renal Therapies Group | Other | Nationwide |
| Device | CLASS II | Velys Enabling Tech Robotic-Assist Station recalled | Medos International Sarl | Device Malfunction | Nationwide |
| Device | CLASS II | Philips Ingenuity CT recalled by Philips North America | Philips North America | Device Malfunction | MA |
| Device | CLASS II | 5008X Standard HD Pre-Flush Standard Blood Tubing Set recalled | Fresenius Medical Care Renal Therapies Group | Packaging Defects | Nationwide |
| Device | CLASS II | Medline Convenience Kits containing BD ChloraPrep Clear recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | Halyard medical convenience kits labeled as: ENT recalled | Avid Medical | Sterility | Nationwide |
| Device | CLASS II | Philips Brilliance CT 64: Brilliance CT 64 Channel recalled | Philips North America | Device Malfunction | MA |
| Device | CLASS II | Lux-Dx, Lux-Dx II, Lux-Dx II+ Insertable Cardiac Monitor recalled | Boston Scientific | Device Malfunction | Nationwide |
| Device | CLASS II | Presource Packs Containing CliniClean Pericare Wipes within recalled | Cardinal Health 200 | Other | Nationwide |
| Device | CLASS II | Healon EndoCoat PRO recalled by Johnson & Johnson Surgical | Johnson & Johnson Surgical Vision | Other | Nationwide |
| Device | CLASS II | Presource Packs Containing CliniClean Pericare Wipes within recalled | Cardinal Health 200 | Other | Nationwide |
| Device | CLASS II | 5008X HD/HDF with Twister Blood Tubing Set recalled | Fresenius Medical Care Renal Therapies Group | Packaging Defects | Nationwide |
| Device | CLASS II | Presource Packs Containing CliniClean Pericare Wipes within recalled | Cardinal Health 200 | Other | Nationwide |
| Device | CLASS II | Presource Packs Containing CliniClean Pericare Wipes within recalled | Cardinal Health 200 | Other | Nationwide |
| Device | CLASS II | STA Staclot Protein recalled by Diagnostica Stago | Diagnostica Stago | Potency & Assay | Nationwide |
| Device | CLASS II | Halyard medical convenience kits labeled as: A-P PACK recalled | Avid Medical | Sterility | Nationwide |
| Device | CLASS II | Medline Convenience Kits: Blood Culture Tray Pediatric recalled | Medline Industries | Sterility | Nationwide |
| Drug | CLASS II | Carton label: Mycophenolate Mofetil for injection recalledMycophenolate Mofetil | Mylan Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS II | Clindamycin Phosphate in 0.9% Sodium Chloride Injection recalledClindamycin Phosphate | Baxter Healthcare | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Vancomycin Injection, USP in 5% Dextrose per (5 mg/mL) recalledVancomycin Hydrochloride | Baxter Healthcare | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Clindamycin Injection USP in 5% Dextrose, 900 mg recalledClindamycin Phosphate | Baxter Healthcare | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Vasopressin, in 0.9% Sodium Chloride Injection per/mL) recalledVasopressin In 0.9% Sodium Chloride | Baxter Healthcare | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Vancomycin Injection, USP, in 0.9% Sodium Chloride recalledVancomycin Hydrochloride | Baxter Healthcare | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Famotidine Injection in Sodium Chloride Injection, 20 mg recalledFamotidine | Baxter Healthcare | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS III | Doxylamine Succinate and Pyridoxine HCl Delayed-Release recalledDoxylamine Succinate And Pyridoxine Hydrochloride | Bionpharma | Other | Nationwide |
| Drug | CLASS II | Myxredlin, Insulin Human in 0.9% Sodium Chloride Injection/mL) recalledMyxredlin | Baxter Healthcare | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Broadway Joe's Pain Cream, 3000 gm CBD recalled by Lexia | Lexia | Manufacturing (CGMP) Deviations | CO |
| Drug | CLASS II | Clindamycin Injection USP in 5% Dextrose, 900 mg recalledClindamycin Phosphate | Baxter Healthcare | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | The One Spf 50 Invisible Sunscreen Gel, (Avobenzone recalled | Allies Group | Potency & Assay | Nationwide |
| Drug | CLASS II | Dexmedetomidine Hydrochloride recalled by Baxter Healthcare | Baxter Healthcare | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | The One Spf 50 Invisible Sunscreen Gel, (Avobenzone recalled | Allies Group | Potency & Assay | Nationwide |
| Drug | CLASS II | Clindamycin Injection USP in 5% Dextrose, 600 mg recalledClindamycin Phosphate | Baxter Healthcare | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Nexterone (amiodarone HCI), 360 mg/ (1.8 mg/mL) recalledNexterone | Baxter Healthcare | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Daptomycin, in 0.9% Sodium Chloride Injection, 500 mg recalled | Baxter Healthcare | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Broadway Joe's Pain Cream, (Histamine Dihydrochloride recalled by Lexia | Lexia | Manufacturing (CGMP) Deviations | CO |
| Drug | CLASS II | Pantoprazole Sodium in 0.9% Sodium Chloride Injection recalledPantoprazole Sodium | Baxter Healthcare | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | The One Spf 50 Invisible Sunscreen Gel, (Avobenzone recalled | Allies Group | Potency & Assay | Nationwide |
| Drug | CLASS II | The One Spf 50 Invisible Sunscreen Gel, (Avobenzone recalled | Allies Group | Potency & Assay | Nationwide |
| Drug | CLASS II | traZODone Hydrochloride Tablets, USP, 50 mg recalledTrazodone Hydrochloride | Teva Pharmaceuticals USA | Other | Nationwide |
| Drug | CLASS III | Trokendi XR, (topiramate) extended-release capsules, 50 mg recalled | Supernus Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS II | Cardene IV (Nicardipine Hydrochloride) recalled by Baxter HealthcareCardene Iv | Baxter Healthcare | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Daptomycin, in 0.9% Sodium Chloride Injection, 1,000 mg recalled | Baxter Healthcare | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Vasopressin, in 0.9% Sodium Chloride Injection per/mL) recalledVasopressin In 0.9% Sodium Chloride | Baxter Healthcare | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Clindamycin Injection USP in 5% Dextrose, 900 mg recalledClindamycin Phosphate | Baxter Healthcare | Manufacturing (CGMP) Deviations | Nationwide |
| Food | CLASS I | Ineligible Pork Cracklings Products recalled | El Eden Import Distributor | Processing Deviation | |
| Food | CLASS III | Wonton Noodle recalled by Wonton SpecialistsWonton Specialist | Wonton Specialists | Undeclared Allergens | NJ, NY, PA |
| Food | CLASS I | Item # DIPPIC0205RFS Pico de Gallo 5 lb packaged in round plastic recalledItem | Ron's Home Style Foods | Salmonella | AR, OK, TX |
| Food | CLASS III | Dumpling Skin recalled by Wonton SpecialistsWonton Specialist | Wonton Specialists | Undeclared Allergens | NJ, NY, PA |
| Food | CLASS I | Organic Cheddar Type Seasoning recalled by Savor Seasonings | Savor Seasonings | Undeclared Milk | OH |
| Food | CLASS III | Lo Mein Noodle recalled by Wonton SpecialistsWonton Specialist | Wonton Specialists | Undeclared Allergens | NJ, NY, PA |
| Food | CLASS III | Wonton Skin recalled by Wonton SpecialistsWonton Specialist | Wonton Specialists | Undeclared Allergens | NJ, NY, PA |
| Food | CLASS III | Prince Sesame French Bread recalled by Prince BakeryPrince | Prince Bakery | Undeclared Sesame | NY |
| Food | CLASS I | Item #DIPSAU0205RFS Salsa Autentica 5 lb. packaged in round plastic recalledItem | Ron's Home Style Foods | Salmonella | AR, OK, TX |
| Food | CLASS II | Prince PAN DE Manteca recalled by Prince BakeryPrince PAN | Prince Bakery | Undeclared Milk | NY |
| Food | CLASS I | Lacnola; Small recalled by The Hampton Grocer | The Hampton Grocer | Salmonella | Nationwide |
| Food | CLASS II | Bread Pudding with Vanilla Sauce recalled by Ukrop's Homestyle Foods | Ukrop's Homestyle Foods | Foreign Material | KY, NC, VA |
| Food | CLASS I | Frankie's Organic Plant-Based Puffs Vegan Cheddar recalledFrankie's | Marina Del Rey Foods | Undeclared Milk | 4 states |
| Food | CLASS III | Prince Italian Bread recalled by Prince BakeryPrince | Prince Bakery | Undeclared Sesame | NY |
| Food | CLASS II | Weis (Fresh From the Orchard ) Pasteurized Apple Cider recalledWeis | Weis Markets | Foreign Material | PA |
| Food | CLASS I | Ola-ola Pounded Yam (Iyan) Iyaninstant recalled by FayusOla-ola Pounded | Fayus | Undeclared Milk | 6 states |
| Food | CLASS III | Cooked Noodle recalled by Wonton SpecialistsWonton Specialist | Wonton Specialists | Undeclared Allergens | NJ, NY, PA |
| Food | CLASS III | Pan Fried Noodle recalled by Wonton SpecialistsWonton Specialist | Wonton Specialists | Undeclared Allergens | NJ, NY, PA |
| Food | CLASS II | Bread Pudding with Vanilla Sauce - KIT recalled | Ukrop's Homestyle Foods | Foreign Material | KY, NC, VA |
| Food | CLASS III | Prince Italian Bread recalled by Prince BakeryPrince | Prince Bakery | Undeclared Sesame | NY |
| Food | ANNOUNCED | FI Supplements recalled by Fi Barking LabsFI | Fi Barking Labs | Salmonella | |
| Device | ANNOUNCED | BMC Luna G3 APAP recalled by BMC MedicalBMC | BMC Medical | Device Malfunction | Nationwide |
| Food | ANNOUNCED | Northside Ready to Eat Deli Style Salads and cream cheese recalledMade Fresh Salads, Northside | Made Fresh Salads | Listeria | NY |
| Food | CLASS I | Imported Ready-To-Eat Pork Guanciale Products recalled | Prime Line Distributors Inc. and Ferrarini USA | Listeria | |
| Food | ANNOUNCED | Business Pill, Branch Manager recalled by Supplx.comBusiness Pill, Branch Manager for Men | Supplx.com | Undeclared Allergens | |
| Food | CLASS II | with black screw lid with multi label which reads recalled | Africando Foods | Undeclared Wheat & Gluten | IA, IL, KY |
| Device | CLASS II | Convenience Kits, CV B PACK recalled by American Contract Systems | American Contract Systems | Foreign Material | Nationwide |
| Device | CLASS II | Portrait Core Services recalled by GE Medical Systems | GE Medical Systems Information Technologies | Device Malfunction | MI, NY |
| Device | CLASS II | Convenience Kit, CV B PACK recalled by American Contract Systems | American Contract Systems | Foreign Material | Nationwide |
| Device | CLASS II | Grandio Universal Nano-Hybrid Restorative Material - Capsules 0.25Gm recalled | Henry Schein | Packaging Defects | Nationwide |
| Device | CLASS II | Medline convenience kits labeled as: LAVH, Medline Kit recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | healthmark ProChek-W Protein Test for Robotic Arms recalled | Healthmark Industries | Other | Nationwide |
| Device | CLASS II | Medline convenience kits labeled as recalled by Medline Industries | Medline Industries | Other | Nationwide |
| Device | CLASS II | Philips Incisive CT recalled by Philips Healthcare (Suzhou) Co | Philips Healthcare (Suzhou) | Device Malfunction | Nationwide |
| Device | CLASS II | Fujifilm Synapse Pacs recalled by FUJIFILM Healthcare Americas | Fujifilm Healthcare Americas | Labeling Errors | Nationwide |
| Device | CLASS II | Convenience Kit, CV B PACK recalled by American Contract Systems | American Contract Systems | Foreign Material | Nationwide |
| Device | CLASS II | Medline medical convenience kits, labeled as recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Medline medical convenience kits, labeled as recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Medline convenience kits labeled as: Open Heart Pack, Medline Kit recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Halyard Total Joint recalled by AVID Medical | Avid Medical | Foreign Material | Nationwide |
| Device | CLASS II | IQecg Digital ECG recalled by Midmark | Midmark | Labeling Errors | Nationwide |
| Device | CLASS II | Medline convenience kits labeled as: GYN Robotic CDS, Medline Kit recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | healthmark ProChek-II recalled by Healthmark Industries Co | Healthmark Industries | Other | Nationwide |
| Device | CLASS II | Linvatec Genesys CrossFT Suture Anchor with Disposable Driver recalled | ConMed | Other | Nationwide |
| Device | CLASS II | Halyard Total Joint recalled by AVID Medical | Avid Medical | Foreign Material | Nationwide |
| Device | CLASS II | Fru (Field replaceable unit), Portrait Core Services SW Reload V1.1 recalled | GE Medical Systems Information Technologies | Device Malfunction | MI, NY |
| Device | CLASS II | Medline convenience kits labeled as: Femoral Pack, Medline Kit recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Halyard Total Joint recalled by AVID Medical | Avid Medical | Foreign Material | Nationwide |
| Device | CLASS II | Medline breathing circuits labeled as: Medline Hudson Rci recalled | Medline Industries | Device Malfunction | Nationwide |
| Device | CLASS II | Halyard Total Joint recalled by AVID Medical | Avid Medical | Foreign Material | Nationwide |
| Device | CLASS II | Structur 2 SC Temporary Resin Cartridge Refill 75Gm recalled | Henry Schein | Packaging Defects | Nationwide |
| Device | CLASS II | Medline medical convenience kits, labeled as: Neuro CDS, Medline Kit recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Digital ECG HD+12, HD+15 recalled by Midmark | Midmark | Labeling Errors | Nationwide |
| Device | CLASS II | Onli Hydrophilic Urethral Intermittent Catheter, labeled as recalled | Hollister Ulc | Device Malfunction | Nationwide |
| Device | CLASS II | Medline medical convenience kit labeled as: Trach Tube Kit recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Medline convenience kits labeled as: Major Gyn Pack, Medline Kit recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Portrait Compute And Core Services V1.2 recalled by GE Medical Systems | GE Medical Systems Information Technologies | Device Malfunction | MI, NY |
| Device | CLASS II | Portrait Core Services recalled by GE Medical Systems | GE Medical Systems Information Technologies | Device Malfunction | MI, NY |
| Device | CLASS II | Convenience Kit, D & C PACK recalled by American Contract Systems | American Contract Systems | Foreign Material | Nationwide |
| Device | CLASS II | Halyard Total Joint recalled by AVID Medical | Avid Medical | Foreign Material | Nationwide |
| Device | CLASS II | Halyard Davinci Trucustom Bundle containing Tray Foley W/Statlock recalled | Avid Medical | Foreign Material | Nationwide |
| Device | CLASS II | Medline convenience kits labeled as: LTP Cds-lf, Medline kit recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Halyard Total Joint recalled by AVID Medical | Avid Medical | Foreign Material | Nationwide |
| Device | CLASS II | Medline Hudson Rci, Dbd-circuit,Vent,Inspiratory,Heated,Neo recalled | Medline Industries | Device Malfunction | Nationwide |
| Device | CLASS II | Medline medical convenience kits, labeled as: Sinus Pack-lf recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Alphenix Models Infx-8000C Infx-8000F Infx-8000V This device recalled | Canon Medical System USA | Other | Nationwide |
| Device | CLASS II | Merge PACS and Merge OrthoPACS recalled by Merge Healthcare | Merge Healthcare | Labeling Errors | Nationwide |
| Device | CLASS II | Fresenius Medical Care, 2008T BlueStar Hemodialysis Machine recalled | Fresenius Medical Care Renal Therapies Group | Temperature Abuse | Nationwide |
| Device | CLASS II | Powerseal (in diameter) (long), Curved Jaw Sealer & Divider recalled | Olympus Corporation of the Americas | Labeling Errors | Nationwide |
| Device | CLASS II | Medline convenience kits labeled as: C-section, Medline Kit recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | ORT300, operating room table recalled by IMRIS Imaging | Imris Imaging | Device Malfunction | Nationwide |
| Device | CLASS II | Medline breathing circuits labeled as: Hudson Rci, Circuit recalled | Medline Industries | Device Malfunction | Nationwide |
| Device | CLASS II | ORT200, operating room table recalled by IMRIS Imaging | Imris Imaging | Device Malfunction | Nationwide |
| Device | CLASS II | Medline convenience kits labeled as: Major Procedure, Medline Kit recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Medline convenience kits labeled as recalled by Medline Industries | Medline Industries | Other | Nationwide |
| Device | CLASS II | Medline convenience kits labeled as: Lami Fusion, Medline Kit recalled | Medline Industries | Other | Nationwide |
| Drug | CLASS II | Paxil CR, Paroxetine, Extended-Release Tablets, 37.5mg recalled | Apotex | Potency & Assay | Nationwide |
| Drug | CLASS II | Levothyroxine Sodium Tablets, USP, 112 mcg (0.112 mg) recalledLevothyroxine Sodium | Accord Healthcare | Potency & Assay | Nationwide |
| Drug | CLASS II | Levothyroxine Sodium Tablets, USP, 88 mcg (0.088 mg) recalledLevothyroxine Sodium | Accord Healthcare | Potency & Assay | Nationwide |
| Drug | CLASS II | Levothyroxine Sodium Tablets, USP, 100 mcg (0.1 mg) recalledLevothyroxine Sodium | Accord Healthcare | Potency & Assay | Nationwide |
| Drug | CLASS I | Lactated Ringer's Injection USP Excel container recalledLactated Ringers | B Braun Medical | Particulate Matter | Nationwide |
| Drug | CLASS I | Tyenne (tocilizumab-aazg) Injection, 400 mg/ (20 mg/mL) vial recalledTyenne | Fresenius Kabi USA | Particulate Matter | Nationwide |
| Drug | CLASS II | Levothyroxine Sodium Tablets, USP, 175 mcg (0.175 mg) recalledLevothyroxine Sodium | Accord Healthcare | Potency & Assay | Nationwide |
| Drug | CLASS II | Zicam, Cold Remedy, Medicated Nasal Swabs recalled by Church & Dwight Co | Church & Dwight | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Levothyroxine Sodium Tablets, USP, 150 mcg (0.15 mg) recalledLevothyroxine Sodium | Accord Healthcare | Potency & Assay | Nationwide |
| Drug | CLASS II | Acthar Gel (repository corticotropin injection) multiple-dose vial recalledActhar | Mallinckrodt Hospital Products | Particulate Matter | Nationwide |
| Drug | CLASS II | Levothyroxine Sodium Tablets, USP, 75 mcg (0.075 mg) recalledLevothyroxine Sodium | Accord Healthcare | Potency & Assay | Nationwide |
| Drug | CLASS II | Levothyroxine Sodium Tablets, USP, 300 mcg (0.3 mg) recalledLevothyroxine Sodium | Accord Healthcare | Potency & Assay | Nationwide |
| Drug | CLASS II | Clobetasol Propionate Cream USP, 0.05% tube recalledClobetasol Propionate | Lupin Pharmaceuticals | Other | Nationwide |
| Drug | CLASS II | Levothyroxine Sodium Tablets, USP, 137 mcg (0.137 mg) recalledLevothyroxine Sodium | Accord Healthcare | Potency & Assay | Nationwide |
| Drug | CLASS II | Levothyroxine Sodium Tablets, USP, 25 mcg (0.025 mg) recalledLevothyroxine Sodium | Accord Healthcare | Potency & Assay | Nationwide |
| Drug | CLASS II | Levothyroxine Sodium Tablets, USP, 125 mcg (0.125 mg) recalledLevothyroxine Sodium | Accord Healthcare | Potency & Assay | Nationwide |
| Drug | CLASS II | Levothyroxine Sodium Tablets, USP, 50 mcg (0.05 mg) recalledLevothyroxine Sodium | Accord Healthcare | Potency & Assay | Nationwide |
| Drug | CLASS II | Ramipril Capsules USP, 10 mg recalled by Hikma Pharmaceuticals USARamipril | Hikma Pharmaceuticals USA | Potency & Assay | Nationwide |
| Drug | CLASS II | Levothyroxine Sodium Tablets, USP, 200 mcg (0.2 mg) recalledLevothyroxine Sodium | Accord Healthcare | Potency & Assay | Nationwide |
| Food | CLASS I | bettergoods Pistachio Nut Butter recalled by Botticelli Foodsbettergoods | Botticelli Foods | Salmonella | 19 states |
| Food | CLASS II | Mehadrin Chocolate Leben recalled by Upstate Niagara CooperativeMehadrin | Upstate Niagara Cooperative | Processing Deviation | NJ |
| Food | CLASS I | Pepper Jalapeno Break recalled by Sirna and Sons ProduceSirna | Sirna and Sons Produce | Salmonella | OH, PA |
| Food | CLASS II | A-L Complex Herbal Supplement May Contain Nuts recalledByron | Byron White Formulas | Undeclared Tree Nuts | 50 states |
| Food | CLASS II | Outshine Fruit Bars Tangerine recalled by Dreyer's Grand Ice CreamOutshine | Dreyer's Grand Ice Cream | Foreign Material | 33 states |
| Food | CLASS II | A-P Herbal Supplement May Contain Nuts recalled by Byron White FormulasByron | Byron White Formulas | Undeclared Tree Nuts | 50 states |
| Food | CLASS I | Jalapeno Ranch recalled by Jaime's Foods ATX | Jaime's Foods ATX | Undeclared Egg | TX |
| Food | CLASS I | Black And White Glutinous Rice Balls With Black Sesame Filling recalled | Khong Guan | Undeclared Peanuts | 8 states |
| Food | CLASS II | Outshine Fruit Bars Strawberry, Pineapple, Grape, Tangerine recalledOutshine | Dreyer's Grand Ice Cream | Foreign Material | 33 states |
| Food | CLASS II | Horizon Organic ORG Asep Choc Milk 1% recalledHorizon | Horizon Organic Dairy | Mold | Nationwide |
| Food | CLASS II | Eridanous Greek Style Shortbread Cookies recalled by Lidl US TRADINGEridanous | Lidl US TRADING | Undeclared Wheat & Gluten | 10 states |
| Food | CLASS II | Outshine Fruit Bars Black Cherry recalled by Dreyer's Grand Ice CreamOutshine | Dreyer's Grand Ice Cream | Foreign Material | 33 states |
| Food | CLASS II | Eridanous Greek Style Shortbread Cookies recalled by Lidl US TRADINGEridanous | Lidl US TRADING | Undeclared Wheat & Gluten | 10 states |
| Food | CLASS II | Outshine Fruit Bars Strawberry recalled by Dreyer's Grand Ice CreamOutshine | Dreyer's Grand Ice Cream | Foreign Material | 33 states |
| Food | CLASS II | Marketside Tomato Bisque Soup Kit, Tomato Bisque recalledMarketside | Cuisine, Kettle | Listeria | 12 states |
| Food | CLASS I | Addall XR Shot, liquid dietary supplement recalled by ZMB EnterprisesAddall XR | ZMB Enterprises | Hidden Drug Ingredients | CA |
| Food | CLASS II | Outshine Fruit Bars Grape recalled by Dreyer's Grand Ice CreamOutshine | Dreyer's Grand Ice Cream | Foreign Material | 33 states |
| Food | CLASS II | Outshine Fruit Bar Watermelon recalled by Dreyer's Grand Ice CreamOutshine | Dreyer's Grand Ice Cream | Foreign Material | 33 states |
| Food | CLASS II | A-fng Herbal Supplement May Contain Nuts recalledByron | Byron White Formulas | Undeclared Tree Nuts | 50 states |
| Food | CLASS I | Glutinous Rice Balls with Black Sesame Filling recalled by Khong Guan | Khong Guan | Undeclared Peanuts | 8 states |
| Food | CLASS I | Sura Tanmen Hot and Sour Flavor Premium Japanese Noodles & Soup Base recalledSura Tanmen | H & U | Undeclared Fish & Shellfish | HI |