| Food | HEALTH ALERT | White Chicken Chili recalled by FSIS | FSIS | Foreign Material | |
| Food | CLASS III | Liquid Egg Products recalled by Cargill Kitchen Solutions | Cargill Kitchen Solutions | Processing Deviation | |
| Device | CLASS II | Vericis, Merge Cardio recalled by Merge Healthcare | Merge Healthcare | Device Malfunction | WI |
| Device | CLASS II | Proxima Drape labeled as Face Lift recalled by MEDLINE INDUSTRIES, LP | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS I | smiths medical ProPort Plastic Venous Access System recalled | Smiths Medical ASD | Foreign Material | MN |
| Device | CLASS I | smiths medical ProPort Plastic Venous Access System recalled | Smiths Medical ASD | Foreign Material | MN |
| Device | CLASS II | Total Hip Pack recalled by American Contract Systems | American Contract Systems | Sterility | Nationwide |
| Device | CLASS II | Microstream Instructions for Use recalled by Oridion Medical 1987 | Oridion Medical 1987 | Device Malfunction | Nationwide |
| Device | CLASS I | smiths medical ProPort Plastic Venous Access System recalled | Smiths Medical ASD | Foreign Material | MN |
| Device | CLASS II | Laparoscopy Pack recalled by American Contract Systems | American Contract Systems | Sterility | Nationwide |
| Device | CLASS II | Laparoscopy Pack recalled by American Contract Systems | American Contract Systems | Sterility | Nationwide |
| Device | CLASS II | EAR PACK recalled by American Contract Systems | American Contract Systems | Sterility | Nationwide |
| Device | CLASS II | Laceration Tray recalled by American Contract Systems | American Contract Systems | Sterility | Nationwide |
| Device | CLASS II | DxI 9000 Access Immunoassay Analyzer recalled by Beckman Coulter | Beckman Coulter | Potency & Assay | Nationwide |
| Device | CLASS II | Neuro Ir Tray recalled by American Contract Systems | American Contract Systems | Sterility | Nationwide |
| Device | CLASS II | Spine Lumbar Pack recalled by American Contract Systems | American Contract Systems | Sterility | Nationwide |
| Device | CLASS II | Major Diep recalled by American Contract Systems | American Contract Systems | Sterility | Nationwide |
| Device | CLASS II | Introcan Safety 3 Closed IV Catheter.., PUR, Winged recalled | B Braun Medical | Packaging Defects | 16 states |
| Device | CLASS II | Modular Stem cylindrical, Tilastan¿, press-fit cementless recalled | Waldemar Link GmbH & Co. KG (Mfg Site) | Other | Nationwide |
| Device | CLASS II | Proxima Drape labeled as Drape C-section W/ Window recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | IsoLoc Short Profile Prostate Immobilization Treatment recalled | Angiodynamics | Labeling Errors | Nationwide |
| Device | CLASS II | Medline procedure kits labeled as: C Section, Pack Number DYNJ909098 recalled | Medline Industries LP - Northfield | Foreign Material | Nationwide |
| Device | CLASS II | Cv Basic Pump Pack recalled by American Contract Systems | American Contract Systems | Sterility | Nationwide |
| Device | CLASS II | Medline procedure kits labeled as: EYE PACK, Pack Number VAL038BSCLC recalled | Medline Industries LP - Northfield | Foreign Material | Nationwide |
| Device | CLASS II | Synapse PACS recalled by FUJIFILM Healthcare Americas | Fujifilm Healthcare Americas | Device Malfunction | 30 states |
| Device | CLASS II | Open Heart A Pack recalled by American Contract Systems | American Contract Systems | Sterility | Nationwide |
| Device | CLASS II | Proxima Drape labeled as Ent-plastics Pack recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | Access 2 Immunoassay Analyzer recalled by Beckman Coulter | Beckman Coulter | Device Malfunction | Nationwide |
| Device | CLASS II | BD Pyxis: Anesthesia Station ES recalled by CareFusion 303 | CareFusion 303 | Device Malfunction | Nationwide |
| Device | CLASS II | DxI 9000 Access Immunoassay Analyzer recalled by Beckman Coulter | Beckman Coulter | Device Malfunction | Nationwide |
| Device | CLASS II | Thoracic Pack recalled by American Contract Systems | American Contract Systems | Sterility | Nationwide |
| Device | CLASS II | Proxima Drape labeled as Minor Pack and Laparoscopy recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | Microstream Instructions for Use recalled by Oridion Medical 1987 | Oridion Medical 1987 | Device Malfunction | Nationwide |
| Device | CLASS II | Microstream Instructions for Use recalled by Oridion Medical 1987 | Oridion Medical 1987 | Device Malfunction | Nationwide |
| Device | CLASS I | smiths medical ProPort Plastic Venous Access System recalled | Smiths Medical ASD | Foreign Material | MN |
| Device | CLASS II | AV Fistula recalled by American Contract Systems | American Contract Systems | Sterility | Nationwide |
| Device | CLASS II | Capnocheck BCI Airway Adapter recalled by Smiths Medical ASD | Smiths Medical ASD | Labeling Errors | Nationwide |
| Device | CLASS I | smiths medical ProPort Low Profile Plastic Venous Access recalled | Smiths Medical ASD | Foreign Material | MN |
| Device | CLASS II | Origin Data Management recalled by Brainlab AG | Brainlab | Device Malfunction | Nationwide |
| Device | CLASS II | C-section Pps recalled by American Contract Systems | American Contract Systems | Sterility | Nationwide |
| Device | CLASS I | smiths medical ProPort Plastic Venous Access System recalled | Smiths Medical ASD | Foreign Material | MN |
| Device | CLASS II | General Angio Pack recalled by American Contract Systems | American Contract Systems | Sterility | Nationwide |
| Device | CLASS II | Modular Stem cylindrical, Tilastan¿, press-fit cementless recalled | Waldemar Link GmbH & Co. KG (Mfg Site) | Other | Nationwide |
| Device | CLASS II | Uro Robotic Pack recalled by American Contract Systems | American Contract Systems | Sterility | Nationwide |
| Device | CLASS II | Capnocheck BCI Airway Adapter recalled by Smiths Medical ASD | Smiths Medical ASD | Labeling Errors | Nationwide |
| Device | CLASS II | Born On Arrival Kit recalled by American Contract Systems | American Contract Systems | Sterility | Nationwide |
| Device | CLASS II | Comprehensive Shoulder Stem recalled by Zimmer Orthopedics | Zimmer Orthopedics Manfacturing Limited-galway | Other | Nationwide |
| Device | CLASS II | Cysto Pack recalled by American Contract Systems | American Contract Systems | Sterility | Nationwide |
| Device | CLASS I | smiths medical ProPort Plastic Venous Access System recalled | Smiths Medical ASD | Foreign Material | MN |
| Device | CLASS II | Helix Elite" Inactivated Standard recalled by Microbiologics | Microbiologics | Potency & Assay | Nationwide |
| Device | CLASS II | Proxima Drape labeled as Head And Neck Osis recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | Microstream Instructions for Use recalled by Oridion Medical 1987 | Oridion Medical 1987 | Device Malfunction | Nationwide |
| Device | CLASS II | Vein Tray recalled by American Contract Systems | American Contract Systems | Sterility | Nationwide |
| Device | CLASS II | Modular Stem cylindrical, Tilastan¿, press-fit cementless recalled | Waldemar Link GmbH & Co. KG (Mfg Site) | Other | Nationwide |
| Device | CLASS II | Proxima Drape labeled as Universal Davinci Robotic P. recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | Microstream Instructions for Use recalled by Oridion Medical 1987 | Oridion Medical 1987 | Device Malfunction | Nationwide |
| Device | CLASS I | smiths medical ProPort Plastic Venous Access System recalled | Smiths Medical ASD | Foreign Material | MN |
| Device | CLASS II | Candida ID Antigen, REAG, AG recalled by Immuno-Mycologics | Immuno-Mycologics | Other | Nationwide |
| Device | CLASS II | Vericis, Merge Cardio recalled by Merge Healthcare | Merge Healthcare | Device Malfunction | WI |
| Device | CLASS I | smiths medical ProPort Plastic Venous Access System recalled | Smiths Medical ASD | Foreign Material | MN |
| Device | CLASS II | Crani Pack recalled by American Contract Systems | American Contract Systems | Sterility | MI |
| Device | CLASS II | Labor & Delivery Pps recalled by American Contract Systems | American Contract Systems | Sterility | Nationwide |
| Device | CLASS II | Dr Diulus Injection Pack recalled by American Contract Systems | American Contract Systems | Sterility | Nationwide |
| Device | CLASS II | Merge Cardio recalled by Merge Healthcare | Merge Healthcare | Device Malfunction | WI |
| Device | CLASS II | Cysto , Model No SACY80R recalled by American Contract Systems | American Contract Systems | Sterility | Nationwide |
| Device | CLASS II | Laparoscopy Pack recalled by American Contract Systems | American Contract Systems | Sterility | Nationwide |
| Device | CLASS II | Laceration Tray recalled by American Contract Systems | American Contract Systems | Sterility | Nationwide |
| Device | CLASS II | HIP Scope recalled by American Contract Systems | American Contract Systems | Sterility | Nationwide |
| Device | CLASS I | smiths medical ProPort Plastic Venous Access System recalled | Smiths Medical ASD | Foreign Material | MN |
| Device | CLASS II | Open Heart Adult - Side recalled by American Contract Systems | American Contract Systems | Sterility | Nationwide |
| Device | CLASS II | Vericis, Merge Cardio recalled by Merge Healthcare | Merge Healthcare | Device Malfunction | WI |
| Device | CLASS II | Microstream Instructions for Use recalled by Oridion Medical 1987 | Oridion Medical 1987 | Device Malfunction | Nationwide |
| Device | CLASS II | Delivery Pack recalled by American Contract Systems | American Contract Systems | Sterility | Nationwide |
| Device | CLASS II | Diagnostic Neuro Ir Tray recalled by American Contract Systems | American Contract Systems | Sterility | Nationwide |
| Device | CLASS II | Vericis, Merge Cardio recalled by Merge Healthcare | Merge Healthcare | Device Malfunction | WI |
| Device | CLASS II | Proxima Drape labeled as Ortho Trauma Cds recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS I | smiths medical ProPort Low Profile Plastic Venous Access recalled | Smiths Medical ASD | Foreign Material | MN |
| Device | CLASS II | Zebra Thermal Barcode Printer GX430t recalled by Remel | Remel | Other | 17 states |
| Device | CLASS II | C-section Pack recalled by American Contract Systems | American Contract Systems | Sterility | Nationwide |
| Device | CLASS II | General Laparoscopic Pack-lf recalled by American Contract Systems | American Contract Systems | Sterility | Nationwide |
| Device | CLASS I | smiths medical ProPort Plastic Venous Access System recalled | Smiths Medical ASD | Foreign Material | MN |
| Device | CLASS II | Proxima Drape labeled as Pack,Basic,Sirus,V,5/CS recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | Central Line Picc recalled by American Contract Systems | American Contract Systems | Sterility | Nationwide |
| Device | CLASS II | Microstream Instructions for Use recalled by Oridion Medical 1987 | Oridion Medical 1987 | Device Malfunction | Nationwide |
| Device | CLASS II | Labor & Delivery Pack recalled by American Contract Systems | American Contract Systems | Sterility | Nationwide |
| Device | CLASS II | Microstream Instructions for Use recalled by Oridion Medical 1987 | Oridion Medical 1987 | Device Malfunction | Nationwide |
| Device | CLASS II | Microstream Instructions for Use recalled by Oridion Medical 1987 | Oridion Medical 1987 | Device Malfunction | Nationwide |
| Device | CLASS II | Microstream Instructions for Use recalled by Oridion Medical 1987 | Oridion Medical 1987 | Device Malfunction | Nationwide |
| Device | CLASS II | Major Vascular Pack recalled by American Contract Systems | American Contract Systems | Sterility | Nationwide |
| Drug | CLASS II | Duloxetine Delayed-Release Capsules, USP, 30 mg recalled | Rising Pharma Holding | Nitrosamine Impurity | Nationwide |
| Drug | CLASS II | Prasugrel Tablets, 5 mg recalled by Golden State Medical SupplyPrasugrel | Golden State Medical Supply | Potency & Assay | Nationwide |
| Drug | CLASS II | Cinacalcet Hydrochloride Tablets 30 mg recalled | Slate Run Pharmaceuticals | Nitrosamine Impurity | Nationwide |
| Drug | CLASS II | Levothyroxine Sodium Tablets, USP, 150 mcg (0.15 mg) recalledLevothyroxine Sodium | Mylan Institutional | Potency & Assay | Nationwide |
| Drug | CLASS II | Neupogen (filgrastim) For Injection, 480 mcg recalled by AmgenNeupogen | Amgen | Potency & Assay | Nationwide |
| Drug | CLASS I | Vitality, Fast Acting Male Enhancement Product recalled | One Source Nutrition Inc | Labeling Errors | Nationwide |
| Drug | CLASS II | Walgreens Maximum Strength Tinted Acne Treatment Cream recalled | Fruit Of The Earth | Benzene | Nationwide |
| Drug | CLASS II | Medline Alcohol Prep Pads, 70% Isopropyl Alcohol recalledMedline Alcohol Prep | Medline Industries LP - Northfield | Potency & Assay | Nationwide |
| Drug | CLASS II | Curad Alcohol Prep Pads, Sterile, Medium, 2-Ply, Contents recalledCurad Alcohol Prep Pads | Medline Industries LP - Northfield | Potency & Assay | Nationwide |
| Drug | CLASS II | Cinacalcet Hydrochloride Tablets 60 mg recalled | Slate Run Pharmaceuticals | Nitrosamine Impurity | Nationwide |
| Drug | CLASS II | Levothyroxine Sodium Tablets, USP, 125 mcg (0.125 mg) recalledLevothyroxine Sodium | Mylan Institutional | Potency & Assay | Nationwide |
| Drug | CLASS II | Ciprofloxacin Ophthalmic Solution USP, 0.3% as base, package recalledCiprofloxacin | FDC | Packaging Defects | Nationwide |
| Drug | CLASS II | Prasugrel Tablets, USP, 5 mg recalled by Mylan PharmaceuticalsPrasugrel | Mylan Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS II | Neupogen (filgrastim) For Injection, 300mcg/ Single Dose Vials recalledNeupogen | Amgen | Potency & Assay | Nationwide |
| Drug | CLASS II | CVS Health Concealing Acne Treatment Cream, CVS recalled | Fruit Of The Earth | Benzene | Nationwide |
| Food | CLASS I | Berry Buddies recalled by Naturipe Value Added FreshBerry Buddies | Naturipe Value Added Fresh | Undeclared Allergens | 13 states |
| Food | CLASS II | Chocolate Peanut Butter Protein Balls recalled by Prep'd CDA | Prep'd CDA | Undeclared Soy | ID, WA |
| Food | CLASS II | Chef's Line US Foods, 3 Grain Slider , Product in a in a cardboard recalledChef's Line | The Fillo Factory | Foreign Material | 5 states |
| Food | CLASS II | Hot Ones Verde, Los Calientes Hot Sauce, BY Heatonist;, and sizes recalledOnes | The Karma Sauce Company | Foreign Material | 4 states |
| Food | CLASS I | Daily Veggies Enoki Mushroom recalled by New Age InternationalDaily Veggies | New Age International | Listeria | NY |
| Food | CLASS I | Ready Care Vanilla Shake Plus recalled by Lyons Magnus | Lyons Magnus | Listeria | Nationwide |
| Food | CLASS I | Ready Care Strawberry Banana Shake No Sugar Added recalled | Lyons Magnus | Listeria | Nationwide |
| Food | CLASS I | Ready Care Chocolate Shake Plus recalled by Lyons Magnus | Lyons Magnus | Listeria | Nationwide |
| Food | CLASS II | Hot Ones Rojo, Los Calientes Hot Sauce, BY Heatonist recalledOnes | The Karma Sauce Company | Foreign Material | 4 states |
| Food | CLASS II | Domna's Bakery 24 PC Baklava Tray recalled by Optima FoodsDomna's | Optima Foods | Undeclared Milk | NY |
| Food | CLASS II | Madras Curry Powder recalled by Trong Food InternationalMadras Curry | Trong Food International | Lead & Heavy Metals | DC, MD |
| Food | CLASS II | Chef's Line US Foods, Black Bean Burger, Product in a in a cardboard recalledChef's Line | The Fillo Factory | Foreign Material | 5 states |
| Food | CLASS II | Chef's Line US Foods, 3 Grain Burger -, Product in a in a cardboard recalledChef's Line | The Fillo Factory | Foreign Material | 5 states |
| Food | CLASS I | Ready Care Chocolate Shake recalled by Lyons Magnus | Lyons Magnus | Listeria | Nationwide |
| Food | CLASS I | Ready Care Vanilla Shake recalled by Lyons Magnus | Lyons Magnus | Listeria | Nationwide |
| Food | CLASS II | Dried Longan Pulp recalled by Growland | Growland | Undeclared Sulfites | 7 states |
| Food | CLASS I | Ready Care Vanilla Shake No Sugar Added recalled by Lyons Magnus | Lyons Magnus | Listeria | Nationwide |
| Food | CLASS I | Ready Care Chocolate Shake No Sugar Added recalled by Lyons Magnus | Lyons Magnus | Listeria | Nationwide |
| Food | CLASS I | Ready Care Strawberry Shake Plus recalled by Lyons Magnus | Lyons Magnus | Listeria | Nationwide |
| Food | CLASS II | emd Oysterettes (oyster crackers in polypropylene film) recalled | Dairy State Foods | Foreign Material | MI |
| Food | CLASS II | Happy Farms by ALDI Colby Jack recalled by Great Lakes Cheese CoHappy | Great Lakes Cheese Co | Foreign Material | 4 states |
| Food | CLASS I | Ready Care Strawberry Shake recalled by Lyons Magnus | Lyons Magnus | Listeria | Nationwide |
| Food | CLASS I | Ready Care Strawberry Shake No Sugar Added recalled by Lyons Magnus | Lyons Magnus | Listeria | Nationwide |
| Food | CLASS I | Ready-To-Eat Beef Stick Products recalled by Idaho Smokehouse Partners | Idaho Smokehouse Partners | Foreign Material | |
| Device | CLASS II | Numerous models of nonsterile hemostatic forceps: (1) REF BH198R recalled | Aesculap | Device Malfunction | Nationwide |
| Device | CLASS II | GE Healthcare Revolution Apex Elite, System, X-ray recalled | GE Medical Systems | Packaging Defects | WI |
| Device | CLASS II | COR Disposable Kit w/ Perpendicularity recalled | DePuy Mitek, Inc., a Johnson & Johnson | Other | Nationwide |
| Device | CLASS II | GE Healthcare Revolution Apex Plus, System, X-ray recalled | GE Medical Systems | Packaging Defects | WI |
| Device | CLASS II | Numerous models of nonsterile hemostatic forceps: (1) REF FB458R recalled | Aesculap | Device Malfunction | Nationwide |
| Device | CLASS II | GE Healthcare Revolution Apex Expert, System, X-ray recalled | GE Medical Systems | Packaging Defects | WI |
| Device | CLASS I | BD Care Coordination Engine (CCE) Infusion Adapter recalled | CareFusion 303 | Device Malfunction | 21 states |
| Device | CLASS II | Pump, Blood, Cardiopulmonary Bypass, Non-Roller Type recalled | Spectrum Medical | Packaging Defects | Nationwide |
| Device | CLASS II | COR Disposable Kit Cartilage Transplant System recalled | DePuy Mitek, Inc., a Johnson & Johnson | Other | Nationwide |
| Device | CLASS II | GE Healthcare Revolution CT ES, System, X-ray, Tomography, Computed recalled | GE Medical Systems | Packaging Defects | WI |
| Device | CLASS II | Z1 Femoral Hip System, Product Number recalled by Zimmer | Zimmer | Other | Nationwide |
| Device | CLASS II | GE Healthcare Revolution CT, System, X-ray, Tomography, Computed recalled | GE Medical Systems | Packaging Defects | WI |
| Device | CLASS II | Da Vinci 5 Assy,DV5 Console,IS5000 Foot Tray Pedals recalled | Intuitive Surgical | Device Malfunction | Nationwide |
| Device | CLASS II | GE Healthcare Revolution Apex Select, System, X-ray recalled | GE Medical Systems | Packaging Defects | WI |
| Device | CLASS II | Numerous models of nonsterile hemostatic forceps: (1) REF BH100R recalled | Aesculap | Device Malfunction | Nationwide |
| Device | CLASS I | Portex Endotracheal Tube recalled by Smiths Medical ASD | Smiths Medical ASD | Other | Nationwide |
| Device | CLASS II | GE Healthcare Revolution Apex, System, X-ray, Tomography, Computed recalled | GE Medical Systems | Packaging Defects | WI |
| Device | CLASS II | Numerous models of nonsterile hemostatic forceps: (1) REF BJ500R recalled | Aesculap | Device Malfunction | Nationwide |
| Device | CLASS II | TruScan Body recalled by TruAbutment | TruAbutment | Device Malfunction | 16 states |
| Device | CLASS II | ZOLL Powerheart G5 AED recalled by ZOLL Medical | Zoll Medical | Temperature Abuse | Nationwide |
| Device | CLASS II | ZOLL Powerheart G5 AED recalled by ZOLL Medical | Zoll Medical | Temperature Abuse | Nationwide |
| Device | CLASS II | Vista Brite Tip, Judkins Right recalled by Cordis US | Cordis US | Other | WA |
| Device | CLASS II | ZOLL Powerheart G5 AED recalled by ZOLL Medical | Zoll Medical | Temperature Abuse | Nationwide |
| Device | CLASS II | Spectral CT on Rails recalled by Philips Medical Systems | Philips Medical Systems Nederl | Device Malfunction | MN |
| Device | CLASS II | DxI 9000 Access Immunoassay Analyzer recalled by Beckman Coulter | Beckman Coulter | Potency & Assay | Nationwide |
| Device | CLASS I | BD Alaris Systems Manager recalled by CareFusion 303 | CareFusion 303 | Device Malfunction | 21 states |
| Device | CLASS II | ZOLL Powerheart G5 AED recalled by ZOLL Medical | Zoll Medical | Temperature Abuse | Nationwide |
| Device | CLASS II | Numerous models of nonsterile hemostatic forceps: (1) REF BH951R recalled | Aesculap | Device Malfunction | Nationwide |
| Device | CLASS II | CardiFocus Heartlight X3 Catheter- Intended recalled by CardioFocus | CardioFocus | Sterility | Nationwide |
| Device | CLASS I | Aortic Root Cannula: Dlp Aortic Root Cannula A. Cannula recalled | Medtronic Perfusion Systems | Other | Nationwide |
| Device | CLASS II | CinchLock Flex Knotless Anchor with Inserter and Suture recalled | Stryker | Device Malfunction | Nationwide |
| Drug | CLASS II | Voriconazole Container Description: voriconazole The product recalled | Aspen Biopharma Labs | Manufacturing (CGMP) Deviations | FL |
| Drug | CLASS I | BD ChloraPrep Clear Applicators recalled by CareFusion 213Chloraprep One-step | CareFusion 213 | Sterility | Nationwide |
| Drug | CLASS II | Kids by babyganics SPF 50 totally tropical recalled | Johnson S C and Son | Packaging Defects | Nationwide |
| Drug | CLASS I | Potassium Chloride Inj., 20 mEq total in flexible container recalledPotassium Chloride | ICU Medical | Labeling Errors | Nationwide |
| Drug | CLASS II | Latanoprost recalled by Aspen Biopharma Labs Pvt | Aspen Biopharma Labs | Manufacturing (CGMP) Deviations | FL |
| Drug | CLASS II | Walgreens, Acne Control Cleanser recalled by Sigan Industries Group | Sigan Industries Group | Benzene | Nationwide |
| Drug | CLASS II | Duloxetine Delayed-Release Capsules, USP, 60mg recalledDuloxetine | Breckenridge Pharmaceutical | Nitrosamine Impurity | Nationwide |
| Drug | CLASS I | PHENYLephrine added to 0.9% sodium chloride, 40 mg/* (160 mcg/mL) recalled | Central Admixture Pharmacy Services | Particulate Matter | Nationwide |
| Drug | CLASS II | Bimatoprost recalled by Aspen Biopharma Labs Pvt | Aspen Biopharma Labs | Manufacturing (CGMP) Deviations | FL |
| Drug | CLASS II | Sodium Chloride Injection 9%, USP, Single-Dose IV recalled | Nephron Sterile Compounding Center | Sterility | Nationwide |
| Drug | CLASS II | Duloxetine Delayed-Release Capsules, USP, 30mg recalledDuloxetine | Breckenridge Pharmaceutical | Nitrosamine Impurity | Nationwide |
| Drug | CLASS II | Alprostadil Container Description: Amber color recalled | Aspen Biopharma Labs | Manufacturing (CGMP) Deviations | FL |
| Drug | CLASS II | Duloxetine Delayed-Release Capsules, USP, 20mg recalledDuloxetine | Breckenridge Pharmaceutical | Nitrosamine Impurity | Nationwide |
| Drug | CLASS I | Potassium Chloride Inj., 10 mEq total recalled by ICU MedicalPotassium Chloride | ICU Medical | Other | Nationwide |
| Drug | CLASS II | Kids by babyganics SPF 50 mineral sunscreen totally recalled | Johnson S C and Son | Packaging Defects | Nationwide |
| Drug | CLASS II | Zapzyt, Acne Treatment Gel, 10% benzoyl peroxide Gel recalledZapzyt Acne Treatment Gel | Denison Pharmaceuticals | Benzene | Nationwide |
| Drug | CLASS III | Livalo (pitavatstatin) tablets, 4 mg recalledLivalo | Kowa Pharmaceuticals America | Other | OH, PA, TX |
| Drug | CLASS II | Finasteride recalled by Aspen Biopharma Labs Pvt | Aspen Biopharma Labs | Manufacturing (CGMP) Deviations | FL |
| Drug | CLASS II | Chlorambucil Container Description: The product recalled | Aspen Biopharma Labs | Manufacturing (CGMP) Deviations | FL |
| Drug | CLASS II | Unisom, SleepMelts, Diphenhydramine HCl tablets, 25 mg recalled | Chattem | Nitrosamine Impurity | Nationwide |
| Food | CLASS II | Trader Joe's branded Solid Light Yellowfin Tuna recalledTrader Joe's | Chicken of the Sea; Thai Union | Botulism | Nationwide |
| Food | CLASS II | Trader Joe's branded Solid White Albacore Tuna in water, Low sodium recalledTrader Joe's | Chicken of the Sea; Thai Union | Botulism | Nationwide |
| Food | CLASS II | Trader Joe's branded Solid White Albacore Tuna in Water, salt added recalledTrader Joe's | Chicken of the Sea; Thai Union | Botulism | Nationwide |
| Food | CLASS II | Coyote Valley Sour Cream & Onion Chips recalled by Uncle RaysCoyote Valley | Uncle Rays | Other | NV, OH, TX |
| Food | CLASS I | Raisin Bran muffins recalled by JE Bakery 2019Raisin Bran | JE Bakery 2019 | Undeclared Allergens | MN, WI |
| Food | CLASS II | Van Camp's branded Solid Light Yellowfin in Vegetable oil recalledVan Camp's | Chicken of the Sea; Thai Union | Botulism | Nationwide |
| Food | CLASS II | Organic Acai Bowl with berries, bananas, granola and dried coconut recalled | Stiebs | Foreign Material | 6 states |
| Food | CLASS I | Southwest Salad Kit recalled by Little Leaf FarmsLittle Leaf | Little Leaf Farms | Undeclared Wheat & Gluten | CT, MA, NH |
| Food | CLASS II | Genova branded Yellowfin Tuna in Extra Virgin Olive Oil and Sea Salt recalledGenova | Chicken of the Sea; Thai Union | Botulism | Nationwide |
| Food | CLASS II | Cinnabon Classic Cinnamon Roll International delight Coffee Creamer recalledCinnabon | Danone Wave | Mold | 31 states |
| Food | CLASS II | Genova branded Yellowfin Tuna recalled by Chicken of the Sea; Thai UnionGenova | Chicken of the Sea; Thai Union | Botulism | Nationwide |
| Food | CLASS II | Trader Joe's branded Solid White Albacore Tuna in olive oil recalledTrader Joe's | Chicken of the Sea; Thai Union | Botulism | Nationwide |
| Food | CLASS I | Aleppo Tahini Sesame Paste recalled by Turkana FoodAleppo Tahini | Turkana Food | Salmonella | 23 states |
| Food | CLASS I | Ulker Rulokat Hazelnut Wafers recalled by ZB ImportingUlker Rulokat | ZB Importing | Undeclared Egg | 36 states |
| Food | CLASS II | Trader Joe's branded Solid White Albacore Tuna in Water recalledTrader Joe's | Chicken of the Sea; Thai Union | Botulism | Nationwide |
| Food | CLASS II | HEB branded Solid White Albacore Tuna in water recalledHeb | Chicken of the Sea; Thai Union | Botulism | Nationwide |
| Food | CLASS II | Hazelnut International delight Coffee Creamer recalled by Danone Wave | Danone Wave | Mold | 31 states |
| Food | CLASS I | Mauna Loa Milk Chocolate Covered Macadamias product recalledMauna Loa | Mauna Loa Macadamia Nut Company | Undeclared Tree Nuts | CA, MI |
| Food | CLASS III | Mi More snacks, Coco Bandera, 8 per container recalledMi More | San Miguel Nuts | Undeclared Allergens | NJ |
| Food | CLASS III | Black Beans, Dried recalled by Trinidad Benham | Trinidad Benham | Foreign Material | 4 states |
| Food | CLASS I | Ulker Biskrem Cocoa Biscuit recalled by ZB ImportingUlker Biskrem | ZB Importing | Undeclared Egg | 36 states |
| Food | CLASS II | Ulker Dankek Roll Cake Banana recalled by ZB ImportingUlker Dankek | ZB Importing | Undeclared Wheat & Gluten | 36 states |
| Food | CLASS II | Green Chile Bean Burrito, 15 days refrigerated recalled | Mi Ranchito Foods, Incorporated | Undeclared Milk | NM |
| Food | CLASS II | Ulker Kekstra Mini strawberry recalled by ZB ImportingUlker Kekstra | ZB Importing | Undeclared Milk | 36 states |
| Food | CLASS II | Good & Gather Cut Green Beans recalled by Del Monte FoodsGood | Del Monte Foods | Foreign Material | 21 states |
| Food | CLASS II | Ulker Dankek Roll Cake Chocolate recalled by ZB ImportingUlker Dankek | ZB Importing | Undeclared Egg | 36 states |
| Food | CLASS II | 1.) Market Pantry Soup & Oyster Crackers recalled by Shearer's Foods | Shearer's Foods | Foreign Material | 24 states |
| Food | CLASS II | Genova branded Solid white Tuna recalledGenova | Chicken of the Sea; Thai Union | Botulism | Nationwide |
| Food | CLASS II | Ulker Dankek Roll Cake Strawberry recalled by ZB ImportingUlker Dankek | ZB Importing | Undeclared Milk | 36 states |
| Food | CLASS II | " Spinach Artichoke Dip (Sold Hot) " Spinach Artichoke Dip recalled | HEB | Foreign Material | TX |
| Device | CLASS II | Osstem Implant System - Abutment: ET Multi AbutmentSize recalled | Hiossen | Packaging Defects | Nationwide |
| Device | CLASS II | Philips IntelliSpace Cardiovascular recalled by Philips Medical Systems | Philips Medical Systems Nederl | Device Malfunction | Nationwide |
| Device | CLASS II | Tissue Approximation System (tas) recalled by TAS Medical | TAS Medical | Sterility | Nationwide |
| Device | CLASS II | MiniMed insulin pump recalled by Medtronic MiniMed | Medtronic MiniMed | Other | Nationwide |
| Device | CLASS II | Alcon Custom Pak with Non-Latex Symbol, Pak recalled by Alcon Research | Alcon Research | Sterility | Nationwide |
| Device | CLASS II | DeRoyal REF 71-C5100NS Tubing, Suction, Connector; DeRoyal REF recalled | DeRoyal Industries | Foreign Material | 5 states |
| Device | CLASS I | Varipulse Bi-Directional Ablation Catheter recalled by Biosense Webster | Biosense Webster | Other | 10 states |
| Device | CLASS II | Lumenis Pulse 120H 30 amp recalled | Lumenis | Other | PA |
| Device | CLASS II | MiniMed insulin pump recalled by Medtronic MiniMed | Medtronic MiniMed | Other | Nationwide |
| Device | CLASS II | MiniMed insulin pump recalled by Medtronic MiniMed | Medtronic MiniMed | Other | Nationwide |
| Device | CLASS II | MiniMed insulin pump recalled by Medtronic MiniMed | Medtronic MiniMed | Other | Nationwide |
| Device | CLASS I | Baxter Spectrum IQ Infusion System with Dose IQ Safety recalled | Baxter Healthcare | Device Malfunction | Nationwide |
| Device | CLASS I | Baxter Sigma Spectrum Infusion System (V6 Platform) recalled | Baxter Healthcare | Other | Nationwide |
| Device | CLASS II | Paradigm insulin pump recalled by Medtronic MiniMed | Medtronic MiniMed | Other | Nationwide |
| Device | CLASS II | ET Rigid Abutment (Mini) Size: 4.5D/H 4.0H- Intended recalled by Hiossen | Hiossen | Packaging Defects | Nationwide |
| Device | CLASS II | ET Rigid Abutment (Mini) SIze: 4.5D/H 7.0H - Intended recalled | Hiossen | Packaging Defects | Nationwide |
| Device | CLASS II | MiniMed insulin pump recalled by Medtronic MiniMed | Medtronic MiniMed | Other | Nationwide |
| Device | CLASS II | Paradigm insulin pump recalled by Medtronic MiniMed | Medtronic MiniMed | Other | Nationwide |
| Device | CLASS II | MiniMed insulin pump recalled by Medtronic MiniMed | Medtronic MiniMed | Other | Nationwide |
| Device | CLASS I | Medtronic Pipeline Vantage Embolization Device recalled | Micro Therapeutics | Other | Nationwide |
| Device | CLASS II | ET Rigid Abutment (Mini) Size 4.5D/H 5.0H - Intended recalled by Hiossen | Hiossen | Packaging Defects | Nationwide |
| Device | CLASS II | Paradigm REF: Mmt-712 and Mmt recalled by Medtronic MiniMed | Medtronic MiniMed | Other | Nationwide |
| Device | CLASS II | MiniMed insulin pump recalled by Medtronic MiniMed | Medtronic MiniMed | Other | Nationwide |
| Device | CLASS II | CircuitGuard ThermoFlo Filter -Combined Heat recalled | Kung Shin Plastics | Foreign Material | Nationwide |
| Device | CLASS II | System, Image Processing, Radiological recalled by MIM Software | MIM Software | Device Malfunction | Nationwide |
| Device | CLASS I | Rotarex Atherectomy System and Instructions for Use recalled | Bard Peripheral Vascular | Device Malfunction | Nationwide |
| Device | CLASS II | MiniMed insulin pump recalled by Medtronic MiniMed | Medtronic MiniMed | Other | Nationwide |
| Device | CLASS II | Access Erythropoietin (EPO) recalled by Beckman Coulter | Beckman Coulter | Other | 20 states |
| Device | CLASS II | TBS Osteo TBS iNsight recalled by Medimaps Group | Medimaps Group | Device Malfunction | 24 states |
| Device | CLASS II | Vios Monitoring System Bedside Monitor recalled by Murata Vios | Murata Vios | Other | Nationwide |
| Device | CLASS II | CircuitGuard Bacterial/Viral Filter with Elbow recalled | Kung Shin Plastics | Foreign Material | Nationwide |
| Device | CLASS II | BD BBL TB Stain Kit recalled by Becton Dickinson & | Becton Dickinson | Other | 14 states |
| Device | CLASS I | Medtronic Pipeline Vantage Embolization Device recalled | Micro Therapeutics | Other | Nationwide |
| Device | CLASS II | Osstem Implant System - Abutment ET Multi Abutment Size recalled | Hiossen | Packaging Defects | Nationwide |
| Device | CLASS II | ET Rigid Abutment (Mini) SIze: 4.5D/H 4.0H - Intended recalled | Hiossen | Packaging Defects | Nationwide |
| Device | CLASS II | Aurora Surgiscope System, Sterile recalled by Integra LifeSciences | Integra LifeSciences | Device Malfunction | Nationwide |
| Device | CLASS II | MiniMed insulin pump recalled by Medtronic MiniMed | Medtronic MiniMed | Other | Nationwide |
| Device | CLASS II | Biofill Infiltration Cannula, diameter recalled by Human Med Ag | Human MED | Other | Nationwide |
| Drug | CLASS II | Nelarabine Injection, 250mg/, (5mg/mL) recalledNelarabine | Zydus Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS II | Simethicone 20 mg per Oral Syringe, Delivers:, Oral Drops recalled | Safecor Health | Packaging Defects | Nationwide |
| Drug | CLASS II | Morphine Sulfate 5 mg per Oral Syringe, Delivers:, Oral Solution recalled | Safecor Health | Packaging Defects | Nationwide |
| Drug | CLASS II | Nelarabine Injection, 250mg/, (5mg/mL) recalledNelarabine | Zydus Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS II | Morphine Sulfate Extended-Release Tablets, 100 mg recalledMorphine Sulfate | SUN Pharmaceutical Industries | Potency & Assay | Nationwide |
| Drug | CLASS II | Ferrous Sulfate 7.5 mg Iron/ Oral Syringe, Delivers recalled | Safecor Health | Packaging Defects | Nationwide |
| Drug | CLASS II | Lorazepam 0.5 mg per Oral Syringe, Delivers:, Oral Concentrate recalled | Safecor Health | Packaging Defects | Nationwide |
| Drug | CLASS II | Ergocalciferol - Vitamin D Supplement recalled by Safecor Health | Safecor Health | Packaging Defects | Nationwide |
| Food | CLASS I | Pan de Sal (Spanish Rolls) recalled by Jesse's BakeryPan | Jesse's Bakery | Undeclared Milk | HI |
| Food | CLASS II | Item #96528 and 32899, King Harvest Sundried Tomato Hummus recalledItem | Pacific Coast Fresh | Foreign Material | ID, OR, WA |
| Food | CLASS II | Item #96522, King Harvest Lemon Hummus recalled by Pacific Coast FreshItem | Pacific Coast Fresh | Foreign Material | ID, OR, WA |
| Food | CLASS II | Item #96520 and item #32898, King Harvest Roasted Garlic Hummus recalledItem | Pacific Coast Fresh | Foreign Material | ID, OR, WA |
| Food | CLASS II | Item #96517, King Harvest Chipotle Hummus recalledItem | Pacific Coast Fresh | Foreign Material | ID, OR, WA |
| Food | CLASS II | Pan de Coco (Coconut Rolls) recalled by Jesse's BakeryPan | Jesse's Bakery | Undeclared Milk | HI |
| Food | CLASS II | Item #96518 and #32895, King Harvest Classic Hummus recalledItem | Pacific Coast Fresh | Foreign Material | ID, OR, WA |
| Food | CLASS I | Family Cobb Salad Cobb Salad recalled by JFE Franchising | JFE Franchising | Salmonella | 4 states |
| Food | CLASS I | Garden Salad Family Garden Salad recalled by JFE FranchisingGarden | JFE Franchising | Salmonella | 4 states |
| Food | CLASS II | Orgeat Almond Syrup;; with screw-top lid recalled by A C Calderoni & CoOrgeat | A C Calderoni & Co | Mold | CA |
| Food | CLASS I | Mixed Melon, Cucumber & Tajin Watermelon & Cucumber w/ Tajin recalled | JFE Franchising | Salmonella | 4 states |
| Food | CLASS I | ASIN B084PZ7K98, Amazon Fresh Jumbo Sugar Cookie, product is baked recalledAsin B084PZ7K98 | Amazon Retail | Undeclared Egg | Nationwide |
| Food | CLASS II | Item #96525 and item #32897, King Harvest Roasted Pepper Hummus recalledItem | Pacific Coast Fresh | Foreign Material | ID, OR, WA |
| Food | CLASS II | Item #96521, item #32896, and item #32898, King Harvest Jalapeno recalledItem | Pacific Coast Fresh | Foreign Material | ID, OR, WA |
| Food | CLASS II | Item #96526 and item #32900, King Harvest Toasted Sesame Hummus recalledItem | Pacific Coast Fresh | Foreign Material | ID, OR, WA |
| Food | CLASS I | Chef Salad recalled by JFE FranchisingChef | JFE Franchising | Salmonella | 4 states |
| Food | CLASS II | Item #96507 and item# 32901, King Harvest Balsamic Hummus recalledItem | Pacific Coast Fresh | Foreign Material | ID, OR, WA |
| Food | CLASS II | Noble Made Garlic Parmesan Wing Sauce recalled by Spicin FoodsNoble Made | Spicin Foods | Other | 18 states |
| Food | CLASS II | Item #96524, King Harvest Toasted Onion Hummus recalledItem | Pacific Coast Fresh | Foreign Material | ID, OR, WA |
| Food | CLASS II | Item #96514 and item #32903, King Harvest Black Olive Hummus recalledItem | Pacific Coast Fresh | Foreign Material | ID, OR, WA |
| Food | CLASS II | Item #96527 and item #32902, King Harvest Spinach Hummus recalledItem | Pacific Coast Fresh | Foreign Material | ID, OR, WA |
| Food | CLASS II | Biostime Kids Calm & Sleep Support Fruity Bites Probiotics recalledBiostime Kids | Health and Happiness (H&H) | Foreign Material | CA, IL, TN |
| Food | CLASS I | Vegetable Bowl Small Vegetable Tray Vegetable Bowl Large recalled | JFE Franchising | Salmonella | 4 states |
| Food | CLASS I | ASIN B0CY2RDW5T, Amazon Fresh products recalled by Amazon RetailAsin B0CY2RDW5T | Amazon Retail | Undeclared Egg | Nationwide |
| Food | CLASS I | Cucumber, Lime & Tajin Cucumber recalled by JFE Franchising | JFE Franchising | Salmonella | 4 states |
| Device | CLASS II | A.L.P.S. mvX-P: Anatomic Lat Fib Plate 12H LT- Anatomic recalled | Tyber Medical | Other | Nationwide |
| Device | CLASS II | A.L.P.S. mvX -Anatomic Lat Fib Plate 6H LT- Anatomic recalled | Tyber Medical | Other | Nationwide |
| Device | CLASS II | A.L.P.S. mvX- Medial Tibia Plate 16H Lt-Medial Tibia Plate recalled | Tyber Medical | Other | Nationwide |
| Device | CLASS II | BD Pyxis MedFlex recalled by CareFusion 303 | CareFusion 303 | Other | Nationwide |
| Device | CLASS II | Optima MR360, NMRI system recalled by GE Healthcare (China) Co | GE Healthcare (China) | Other | Nationwide |
| Device | CLASS II | Lifepak 20e recalled by Physio-Control | Physio-Control | Other | WV |
| Device | CLASS II | Signa MR380, Nmri system, Non-US Only recalled | GE Healthcare (China) | Other | Nationwide |
| Device | CLASS II | A.L.P.S. mvX- Anatomic Lat Fib Plate 10H RT- Anatomic recalled | Tyber Medical | Other | Nationwide |
| Device | CLASS I | Vocsn Multi-Function Ventilators: Vocsn+Pro (V+O+C+S+N+Pro, English) recalled | Ventec Life Systems | Labeling Errors | CA, MO, NY |
| Device | CLASS II | Socrates 38 Aspiration Catheter length recalled by Scientia Vascular | Scientia Vascular | Sterility | Nationwide |
| Device | CLASS II | Plato 17 Microcatheter recalled by Scientia Vascular | Scientia Vascular | Sterility | Nationwide |
| Device | CLASS II | IntelePACS (Image Fusion Module) - InteleViewer recalled | Intelerad Medical Systems | Device Malfunction | Nationwide |
| Device | CLASS II | A.L.P.S. mvX- Anatomic Lat Fib Plate 8H RT recalled by Tyber Medical | Tyber Medical | Other | Nationwide |
| Device | CLASS II | BD Pyxis: MedFlex recalled by CareFusion 303 | CareFusion 303 | Device Malfunction | Nationwide |
| Device | CLASS II | 139088-01 Bd Pyxis Medbank Medpass Module 169-151 Bd Pyxis recalled | CareFusion 303 | Other | Nationwide |
| Device | CLASS II | 155288-01 Bd Pyxis Medbank Mini 1fh-1fm 169-137 Bd Pyxis recalled | CareFusion 303 | Other | Nationwide |
| Device | CLASS II | Pentax Medical Video Colonoscope- Intended to provide recalled | Pentax of America | Other | Nationwide |
| Device | CLASS II | DxC 500 AU Clinical Chemistry Analyzer recalled | Beckman Coulter Laboratory Systems (Suzhou) | Labeling Errors | 19 states |
| Device | CLASS II | 139054-01 Bd Pyxis Medflex Mn 1000 10hh-1fm 139055-01 Bd recalled | CareFusion 303 | Other | Nationwide |
| Device | CLASS II | A.L.P.S. mvX- Medial Tibia Plate 6H Rt-Medial Tibia Plate recalled | Tyber Medical | Other | Nationwide |
| Device | CLASS II | A.L.P.S. mvX -Anatomic Lat Fib Plate 4H RT recalled by Tyber Medical | Tyber Medical | Other | Nationwide |
| Device | CLASS II | Leica Biosystems Cryostats CM1950 recalled | Leica Biosystems Nussloch | Device Malfunction | Nationwide |
| Device | CLASS II | Pentax Medical Video Upper GI Scope-Intended to provide recalled | Pentax of America | Other | Nationwide |
| Device | CLASS II | 138913-01 Bd Pyxis Medbank Mini Cr-2hh-1fh-p 169-114 Bd recalled | CareFusion 303 | Other | Nationwide |
| Device | CLASS II | A.L.P.S. mvX- Medial Tibia Plate 16H RT -Medial Tibia Plate recalled | Tyber Medical | Other | Nationwide |
| Device | CLASS II | Signa MR355, Signa MR360, Nmri system recalled | GE Healthcare (China) | Other | Nationwide |
| Device | CLASS II | A.L.P.S. mvX- Anatomic Lat Fib Plate 12H RT- Anatomic recalled | Tyber Medical | Other | Nationwide |
| Device | CLASS II | Pentax Medical Video Processor- Intended to be used recalled | Pentax of America | Other | Nationwide |
| Device | CLASS II | Signa Creator, Signa Explorer, Nmri systems recalled | GE Healthcare (China) | Other | Nationwide |
| Device | CLASS II | A.L.P.S. mvX - Anatomic Lat Fib Plate 4H LT recalled by Tyber Medical | Tyber Medical | Other | Nationwide |
| Device | CLASS II | A.L.P.S. mvX- Anatomic Lat Fib Plate 8H LT recalled by Tyber Medical | Tyber Medical | Foreign Material | Nationwide |
| Device | CLASS II | A.L.P.S. mvX- Anatomic Lat Fib Plate 6H RT recalled by Tyber Medical | Tyber Medical | Other | Nationwide |
| Device | CLASS II | A.L.P.S. mvX- Medial Tibia Plate 10H LT- Medial Tibia Plate recalled | Tyber Medical | Other | Nationwide |
| Device | CLASS II | Anatomic Lat Fib Plate 10H LT Anatomic Lateral Fibula Plate recalled | Tyber Medical | Other | Nationwide |
| Device | CLASS II | A.L.P.S. mvX-Medial Tibia Plate 10H Rt-Medial Tibia Plate recalled | Tyber Medical | Other | Nationwide |
| Device | CLASS II | BD Alaris Pump Module recalled by CareFusion 303 | CareFusion 303 | Other | 50 states |
| Device | CLASS II | A.L.P.S. mvX--Medial Tibia Plate 12H Rt-Medial Tibia Plate recalled | Tyber Medical | Other | Nationwide |
| Device | CLASS II | Brivo MR355, NMRI system recalled by GE Healthcare (China) Co | GE Healthcare (China) | Other | Nationwide |
| Device | CLASS II | ASP Biotrace Auto Read 60 Steam BI Process Challenge Device recalled | Terragene | Other | Nationwide |
| Device | CLASS II | A.L.P.S. mvX-Medial Tibia Plate 6H Lt-Medial Tibia Plate recalled | Tyber Medical | Other | Nationwide |
| Device | CLASS II | A.L.P.S. mvX-Medial Tibia Plate 12H Lt-Medial Tibia Plate recalled | Tyber Medical | Other | Nationwide |
| Drug | CLASS II | ViaMed Alcohol Prep Pads, For External Use Only recalled | Wuxi Medical lnstrument Factory | Sterility | FL |
| Drug | CLASS II | Avastin 1.25 mg/ in Syringe recalled by Turbare Manufacturing | Turbare Manufacturing | Sterility | Nationwide |
| Drug | CLASS II | Estradiol Gel, 0.1%, 0.25 mg/g, 30 packets recalled by Padagis US | Padagis US | Packaging Defects | Nationwide |
| Food | CLASS II | Assorted Chocolate Caramels with kosher sea salt recalled | V Chocolates | Foreign Material | Nationwide |
| Food | CLASS II | 5912MOD-CAU 11" Gluten Free Friendly Cauliflower Shell recalled | Deiorio Foods | Foreign Material | 11 states |
| Food | CLASS II | Beverage Base Lemonade, BIB: Best By 12/12/2025 recalled by OcbwBeverage Base | Ocbw | Undeclared Allergens | 8 states |
| Food | CLASS I | Gerber Snacks for Baby Soothe 'n' Chew Teething Sticks recalledGerber Snacks | Nestle-USA, Inc. (Corporate Office) | Choking Hazard | 46 states |
| Food | CLASS I | Garden Salad recalled by Freshpoint Central FloridaGarden | Freshpoint Central Florida | Undeclared Peanuts | FL, GA |
| Food | CLASS II | Fine Potato Flour, product #20501 recalled by Idaho PacificIdaho Pacific | Idaho Pacific | Undeclared Milk | IL, MI, OR |
| Food | CLASS I | Gerber Snacks for Baby Soothe 'n' Chew Teething Sticks Banana recalledGerber Snacks | Nestle-USA, Inc. (Corporate Office) | Choking Hazard | 46 states |
| Food | CLASS II | Rajbhog Sweets Jelebi Yellow packages recalledRajbhog Sweets | Rajbhog Distributors TX | Undeclared Milk | TX |
| Food | CLASS II | Beverage Base Sweet&Sour, BIB: Best By 12/10/2025 recalled by OcbwBeverage Base | Ocbw | Undeclared Allergens | 8 states |
| Food | CLASS II | Rajbhog Sweets Jelebi Orange packages recalledRajbhog Sweets | Rajbhog Distributors TX | Undeclared Milk | TX |
| Food | CLASS I | Food Service - Mombo s Vanilla Soft Serve Ice Cream Mix recalled | Arizona Foods Group | Undeclared Egg | NV |
| Food | CLASS II | Rajbhog Sweets Jelebi Jaggery packages recalledRajbhog Sweets | Rajbhog Distributors TX | Undeclared Milk | TX |