| Device | CLASS II | EsteemBody Drainable recalled by ConvaTec | ConvaTec | Packaging Defects | Nationwide |
| Device | CLASS II | Centricity Universal Viewer recalled by GE Medical Systems | GE Medical Systems | Device Malfunction | Nationwide |
| Device | CLASS II | Welch Allyn Spot Vision Screener VS100 recalled by Baxter Healthcare | Baxter Healthcare | Device Malfunction | Nationwide |
| Device | CLASS II | ID NOW" Influenza recalled by Abbott Diagnostics Scarborough | Abbott Diagnostics Scarborough | Device Malfunction | Nationwide |
| Device | CLASS II | Centricity Universal Viewer recalled by GE Medical Systems | GE Medical Systems | Device Malfunction | Nationwide |
| Device | CLASS II | Aptima HPV Assay recalled by Hologic | Hologic | Potency & Assay | Nationwide |
| Device | CLASS II | Cub Pediatric Crib recalled by Stryker Medical Division of | Stryker Medical Division of Stryker | Other | Nationwide |
| Device | CLASS II | Artegraft Vascular Graft recalled by LeMaitre Vascular | LeMaitre Vascular | Packaging Defects | Nationwide |
| Device | CLASS II | EsteemBody Drainable recalled by ConvaTec | ConvaTec | Packaging Defects | Nationwide |
| Device | CLASS II | EsteemBody Drainable recalled by ConvaTec | ConvaTec | Packaging Defects | Nationwide |
| Device | CLASS II | STA Liatest D-Di recalled by Diagnostica Stago | Diagnostica Stago | Potency & Assay | Nationwide |
| Device | CLASS II | Centricity Universal Viewer recalled by GE Medical Systems | GE Medical Systems | Device Malfunction | Nationwide |
| Device | CLASS II | Leksell Gamma Knife¿ Perfexion Leksell Gamma Knife¿ Icon" recalled | Elekta | Other | Nationwide |
| Device | CLASS II | MICS3 Angled Sagittal Saw Attachment recalled by Howmedica Osteonics | Howmedica Osteonics | Other | Nationwide |
| Device | CLASS III | Battery Charging Station recalled by Datascope | Datascope | Device Malfunction | Nationwide |
| Drug | CLASS II | Dexamethasone Sodium Phosphate Injection, USP, 100 mg recalledDexamethasone Sodium Phosphate | Somerset Therapeutics | Potency & Assay | Nationwide |
| Drug | CLASS I | Webcol Alcohol Prep pad (70% isopropyl alcohol) 2 ply recalled | Cardinal Health 200 | Sterility | Nationwide |
| Drug | CLASS III | Pitavastatin Tablets, 2 mg recalled by Annora Pharma PrivatePitavastatin Calcium | Annora Pharma Private | Packaging Defects | TN |
| Drug | CLASS II | Children's Ibuprofen Oral Suspension, USP, 100 mg recalledIbuprofen | Strides Pharma | Particulate Matter | Nationwide |
| Drug | CLASS II | Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution 0.2%/0.5%* recalledBrimonidine Tartrate/timolol Maleate Ophthalmic Solution | Apotex | Sterility | Nationwide |
| Food | HEALTH ALERT | Beef and Pork Products recalled by FSIS | FSIS | Undeclared Allergens | |
| Food | CLASS II | Tetas Mireya, Cherry Milkshake (Colita con Leche), i unit Popsicle recalledTetas Mireya | Asukar Foods | Undeclared Allergens | FL |
| Food | CLASS II | Wawa Cookies & Cream Milk (Pint) Store Refrigerated recalledWawa | Wawa Beverage | Foreign Material | 4 states |
| Food | CLASS I | Butter Powder recalled by Bluegrass Ingredients | Bluegrass Ingredients | Salmonella | FL, IL, MD |
| Food | CLASS II | Clover Sonoma Sour Cream recalled by Saputo Cheese UsaClover Sonoma | Saputo Cheese Usa | Packaging Defects | 11 states |
| Food | CLASS II | Greenway Farms of Georgia Garlic Dill Pickles Chips recalledGreenway | BlueFrog Foods | Other | GA |
| Food | CLASS II | Wawa Chocolate Low-fat Milk , (Pint) .Store Refrigerated recalledWawa | Wawa Beverage | Foreign Material | 4 states |
| Food | CLASS I | Product label reads in part as "White Vein Advanced recalledProduct | Shaman Botanicals | Foreign Material | MO |
| Food | CLASS I | Product label reads in part as "White Vein Advanced recalledProduct | Shaman Botanicals | Foreign Material | MO |
| Food | CLASS II | Simply Nature, Spinach Bites retail unit recalledSimply Nature | Dr. Praeger's Sensible Foods | Foreign Material | MD, PA |
| Food | CLASS I | Miss Vickies Spicy Dill Pickle recalled by Frito-lay North AmericaMiss Vickies | Frito-lay North America | Undeclared Allergens | 6 states |
| Food | CLASS II | Clover Sonoma Cottage Cheese Low Fat 2% Milkfat recalledClover Sonoma | Saputo Cheese Usa | Packaging Defects | 11 states |
| Food | CLASS I | Butter-Rich Powder recalled by Bluegrass IngredientsButter-Rich | Bluegrass Ingredients | Salmonella | FL, IL, MD |
| Food | CLASS I | MID EAST Jordanian Zaatar spice mix recalledMID East | Kradjian Importing Company | Undeclared Allergens | CA |
| Food | CLASS I | Zaatar Chickpea Salad recalled by DreamlandDreamland's Zaatar | Dreamland | Undeclared Sesame | WA |
| Food | CLASS II | Wawa Double Dutch Chocolate Milk (Pint) Store Refrigerated recalledWawa Double | Wawa Beverage | Foreign Material | 4 states |
| Food | CLASS III | Multivitamin with Fluoride Chewable Tablets Grape Flavor Rx recalledMultivitamin | Winder Laboratories | Potency & Assay | 25 states |
| Food | CLASS II | Great Value Cottage Cheese Small Curd 4% Milkfat recalledGreat | Saputo Cheese Usa | Packaging Defects | 11 states |
| Food | CLASS II | Greenway Farms of Georgia Jalapeno Dill Pickles Chips recalledGreenway | BlueFrog Foods | Other | GA |
| Food | CLASS II | Great Value Lowfat Cottage Cheese Small Curd 2% Milkfat recalledGreat | Saputo Cheese Usa | Packaging Defects | 11 states |
| Food | CLASS II | Wawa Reduced Fat Milk 2% (Pint) recalled by Wawa BeverageWawa | Wawa Beverage | Foreign Material | 4 states |
| Food | CLASS II | Great Value Fat Free Cottage Cheese Small Curd 0% Milkfat recalledGreat | Saputo Cheese Usa | Packaging Defects | 11 states |
| Food | HEALTH ALERT | Ground Beef Products recalled by White Oak Pastures | White Oak Pastures | Foreign Material | |
| Device | CLASS II | Endo-Model Replacement Plateau; Item Number: 15-0027/16 recalled | Waldemar Link GmbH & Co. KG (Mfg Site) | Other | Nationwide |
| Device | CLASS II | Endo-Model Replacement Plateau; Item Number: 15-0027/12 recalled | Waldemar Link GmbH & Co. KG (Mfg Site) | Other | Nationwide |
| Device | CLASS II | Endo-Model Replacement Plateau; Item Number: 15-8521/11 recalled | Waldemar Link GmbH & Co. KG (Mfg Site) | Other | Nationwide |
| Device | CLASS II | GEM Premier 5000 PAK recalled by Instrumentation Laboratory | Instrumentation Laboratory | Other | Nationwide |
| Device | CLASS II | EndoVive Safety PEG Kit recalled by Boston Scientific | Boston Scientific | Sterility | Nationwide |
| Device | CLASS II | Wondfo Streptococcal A At-Home Self-Test recalled by Altruan | Altruan | Other | Nationwide |
| Device | CLASS II | Endo-Model Replacement Plateau; Item Number: 15-8521/09 recalled | Waldemar Link GmbH & Co. KG (Mfg Site) | Other | Nationwide |
| Device | CLASS III | Penner Pacific Bathing Spa recalled by Penner Patient Care | Penner Patient Care | Device Malfunction | Nationwide |
| Device | CLASS II | Bisaf Strep A Self-Test recalled by Altruan | Altruan | Other | Nationwide |
| Device | CLASS II | Aptus 2.8 TriLock Screw, HD7, 1/Pkg recalled by Medartis AG | Medartis | Device Malfunction | Nationwide |
| Device | CLASS II | Endo-Model SL Connection Component incl. PE-Plateau; Item Number recalled | Waldemar Link GmbH & Co. KG (Mfg Site) | Other | Nationwide |
| Device | CLASS II | GEM Premier recalled by Instrumentation Laboratory | Instrumentation Laboratory | Other | Nationwide |
| Device | CLASS II | GEM Premier 5000 PAK recalled by Instrumentation Laboratory | Instrumentation Laboratory | Other | Nationwide |
| Device | CLASS II | GEM Premier 5000 PAK recalled by Instrumentation Laboratory | Instrumentation Laboratory | Other | Nationwide |
| Device | CLASS II | Clarity II Laser System recalled by Lutronic | Lutronic | Other | Nationwide |
| Device | CLASS II | Medline Surgical Drapes: MDTBTCS6070GN recalled by Medline Industries | Medline Industries | Other | Nationwide |
| Device | CLASS II | Endo-Model Replacement Plateau; Item Number: 15-2836/11 recalled | Waldemar Link GmbH & Co. KG (Mfg Site) | Other | Nationwide |
| Device | CLASS II | Endo-Model SL Connection Component incl. PE-Plateau; Item Number recalled | Waldemar Link GmbH & Co. KG (Mfg Site) | Other | Nationwide |
| Device | CLASS II | Medline Medcrest Surgical Gowns recalled by Medline Industries | Medline Industries | Other | Nationwide |
| Device | CLASS II | GEM Premier recalled by Instrumentation Laboratory | Instrumentation Laboratory | Other | Nationwide |
| Device | CLASS II | Endo-Model Replacement Plateau; Item Number: 15-2835/12 recalled | Waldemar Link GmbH & Co. KG (Mfg Site) | Other | Nationwide |
| Device | CLASS II | IBA Proton Therapy System - Proteus recalled by Ion Beam Applications | Ion Beam Applications | Device Malfunction | Nationwide |
| Device | CLASS III | Penner Pacific Bathing Spa recalled by Penner Patient Care | Penner Patient Care | Device Malfunction | Nationwide |
| Device | CLASS II | Equinoxe Core Instrument Kit recalled by Exactech | Exactech | Other | 19 states |
| Device | CLASS I | Owner's Booklets and Instructions for Use that are used recalled | Trividia Health | Device Malfunction | Nationwide |
| Device | CLASS II | Non-Sterile BD Luer-Lok Tip Syringe Only recalled by Becton Dickinson & | Becton Dickinson | Packaging Defects | Nationwide |
| Device | CLASS II | Clearest Strep-A Cassette Test recalled by Altruan | Altruan | Other | Nationwide |
| Device | CLASS III | Penner Pacific Bathing Spa recalled by Penner Patient Care | Penner Patient Care | Device Malfunction | Nationwide |
| Device | CLASS II | GEM Premier recalled by Instrumentation Laboratory | Instrumentation Laboratory | Other | Nationwide |
| Device | CLASS III | Penner Pacific Bathing Spa recalled by Penner Patient Care | Penner Patient Care | Device Malfunction | Nationwide |
| Device | CLASS II | Endo-Model Replacement Plateau; Item Number: 15-0027/15 recalled | Waldemar Link GmbH & Co. KG (Mfg Site) | Other | Nationwide |
| Device | CLASS III | Penner Pacific Bathing Spa recalled by Penner Patient Care | Penner Patient Care | Device Malfunction | Nationwide |
| Device | CLASS III | Penner Pacific Bathing Spa recalled by Penner Patient Care | Penner Patient Care | Device Malfunction | Nationwide |
| Device | CLASS II | HealthCast "Vital Sync" Remote Patient Monitoring System recalled | Covidien | Device Malfunction | Nationwide |
| Device | CLASS III | Penner Pacific Bathing Spa recalled by Penner Patient Care | Penner Patient Care | Device Malfunction | Nationwide |
| Device | CLASS II | GEM Premier recalled by Instrumentation Laboratory | Instrumentation Laboratory | Other | Nationwide |
| Device | CLASS II | Artelon FlexBand Plus recalled by International Life Sciences | International Life Sciences | Other | Nationwide |
| Device | CLASS II | Medline Unna-z Stretch Zinc Paste Bandage recalled by KOB | KOB | Labeling Errors | IL |
| Device | CLASS II | Artelon Flexband Twist .12 recalled by International Life Sciences | International Life Sciences | Other | Nationwide |
| Device | CLASS II | GEM Premier recalled by Instrumentation Laboratory | Instrumentation Laboratory | Other | Nationwide |
| Device | CLASS II | GEM Premier recalled by Instrumentation Laboratory | Instrumentation Laboratory | Other | Nationwide |
| Device | CLASS I | Owner's Booklets and Instructions for Use that are used recalled | Trividia Health | Device Malfunction | Nationwide |
| Device | CLASS II | GEM Premier 5000 PAK recalled by Instrumentation Laboratory | Instrumentation Laboratory | Other | Nationwide |
| Device | CLASS II | GEM Premier 5000 PAK recalled by Instrumentation Laboratory | Instrumentation Laboratory | Other | Nationwide |
| Device | CLASS II | GEM Premier recalled by Instrumentation Laboratory | Instrumentation Laboratory | Other | Nationwide |
| Device | CLASS II | GEM Premier 5000 PAK recalled by Instrumentation Laboratory | Instrumentation Laboratory | Other | Nationwide |
| Device | CLASS II | Aptus 2.5 TriLock Screw, HD7, 1/Pkg recalled by Medartis AG | Medartis | Device Malfunction | Nationwide |
| Device | CLASS II | Physio Control Infant/Child Reduced Energy Defibrillator Electrodes recalled | Physio-Control | Other | Nationwide |
| Device | CLASS II | DxC 700 AU recalled by Beckman Coulter Mishima K.K | Beckman Coulter Mishima K.K | Device Malfunction | Nationwide |
| Device | CLASS II | GEM Premier 5000 PAK recalled by Instrumentation Laboratory | Instrumentation Laboratory | Other | Nationwide |
| Device | CLASS III | Penner Pacific Bathing Spa recalled by Penner Patient Care | Penner Patient Care | Device Malfunction | Nationwide |
| Device | CLASS III | Penner Pacific Bathing Spa recalled by Penner Patient Care | Penner Patient Care | Device Malfunction | Nationwide |
| Device | CLASS II | Equinoxe Ergo Modular Impactor Handle recalled by Exactech | Exactech | Other | 19 states |
| Device | CLASS II | Medline Kits containing Cardinal Health s Aqua-Seal Chest recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | GEM Premier 5000 PAK recalled by Instrumentation Laboratory | Instrumentation Laboratory | Other | Nationwide |
| Device | CLASS II | GEM Premier recalled by Instrumentation Laboratory | Instrumentation Laboratory | Other | Nationwide |
| Device | CLASS II | Endo-Model Replacement Plateau; Item Number: 15-8521/15 recalled | Waldemar Link GmbH & Co. KG (Mfg Site) | Other | Nationwide |
| Device | CLASS II | GEM Premier recalled by Instrumentation Laboratory | Instrumentation Laboratory | Other | Nationwide |
| Device | CLASS II | GEM Premier recalled by Instrumentation Laboratory | Instrumentation Laboratory | Other | Nationwide |
| Device | CLASS II | Raz-AT (Attendant Tilt) Mobile Shower Commode Chair recalled | Raz Design | Other | Nationwide |
| Device | CLASS II | Endo-Model SL Connection Component incl. PE-Plateau; Item Number recalled | Waldemar Link GmbH & Co. KG (Mfg Site) | Other | Nationwide |
| Device | CLASS I | Owner's Booklets and Instructions for Use that are used recalled | Trividia Health | Device Malfunction | Nationwide |
| Device | CLASS II | Endo-Model Replacement Plateau; Item Number: 15-8030/12 recalled | Waldemar Link GmbH & Co. KG (Mfg Site) | Other | Nationwide |
| Device | CLASS II | GEM Premier recalled by Instrumentation Laboratory | Instrumentation Laboratory | Other | Nationwide |
| Device | CLASS II | Artelon FlexBand Dynamic Matrix recalled by International Life Sciences | International Life Sciences | Other | Nationwide |
| Device | CLASS I | Owner's Booklets and Instructions for Use that are used recalled | Trividia Health | Device Malfunction | Nationwide |
| Device | CLASS II | Chemistry Analyzer Au5800 recalled by Beckman Coulter Mishima K.K | Beckman Coulter Mishima K.K | Device Malfunction | Nationwide |
| Device | CLASS II | GEM Premier 5000 PAK recalled by Instrumentation Laboratory | Instrumentation Laboratory | Other | Nationwide |
| Device | CLASS III | Penner Pacific Bathing Spa recalled by Penner Patient Care | Penner Patient Care | Device Malfunction | Nationwide |
| Device | CLASS II | Endo-Model Replacement Plateau; Item Number: 15-0027/11 recalled | Waldemar Link GmbH & Co. KG (Mfg Site) | Other | Nationwide |
| Drug | CLASS II | Icosapent Ethyl Capsules recalled by Zydus Pharmaceuticals (USA)Icosapent Ethyl | Zydus Pharmaceuticals | Other | Nationwide |
| Food | CLASS I | Caramel Apple Cream Cheese recalled by Made Fresh SaladsSalads | Made Fresh Salads | Listeria | NY |
| Food | CLASS I | Sundried Tomato Cream Cheese recalled by Made Fresh SaladsSalads | Made Fresh Salads | Listeria | NY |
| Food | CLASS I | Tofu Whipped recalled by Made Fresh SaladsSalads | Made Fresh Salads | Listeria | NY |
| Food | CLASS II | Vegetarian Chicken Flavor Ramen Express recalledVegetarian | Palmetto Gourmet Foods | Undeclared Allergens | 32 states |
| Food | CLASS I | Rosabella Moringa recalled by Ambrosia BrandsRosabella | Ambrosia Brands | Salmonella | Nationwide |
| Food | CLASS II | Hortex Mieszanka 9 - skBadnikowa Spring vegetable mix recalledHortex Mieszanka | Polski Ogrod Sp. z o.o | Foreign Material | IL |
| Food | CLASS II | Secondary Packaging: Zhong Hua Chao Mian Noodle Ingredients recalledSecondary Packaging | CNC Noodle | Undeclared Wheat & Gluten | CA, NV |
| Food | CLASS I | Jalapeno Cheddar Cream Cheese recalled by Made Fresh SaladsSalads | Made Fresh Salads | Listeria | NY |
| Food | CLASS I | Walnut Raisin Cream Cheese recalled by Made Fresh SaladsSalads | Made Fresh Salads | Listeria | NY |
| Food | CLASS I | Jalapeno Cream Cheese recalled by Made Fresh SaladsSalads | Made Fresh Salads | Listeria | NY |
| Food | CLASS III | C2O Coconut Water with Pulp recalled by Tipp DistributorsC2o | Tipp Distributors | Labeling Errors | 11 states |
| Food | CLASS II | Coco's Italian Market Heat-n-Eat Fettuccini Alfredo recalledCoco's | Cocos Wholesale and Imports | Undeclared Wheat & Gluten | TN |
| Food | CLASS I | Vegetable Cream Cheese recalled by Made Fresh SaladsSalads | Made Fresh Salads | Listeria | NY |
| Food | CLASS I | Apple Cinnamon Cream Cheese recalled by Made Fresh SaladsSalads | Made Fresh Salads | Listeria | NY |
| Food | CLASS I | Garlic & Herb Cream Cheese recalled by Made Fresh SaladsSalads | Made Fresh Salads | Listeria | NY |
| Food | CLASS II | Vegetarian Chicken Flavor Ramen Express recalledVegetarian | Palmetto Gourmet Foods | Undeclared Allergens | 32 states |
| Food | CLASS I | Blueberry Cream Cheese recalled by Made Fresh SaladsSalads | Made Fresh Salads | Listeria | NY |
| Food | CLASS II | Frozen Raw Bulk Blueberry Crumble Pie (4 pies/case) recalled | Willamette Valley Pie Company | Listeria | IL, OR |
| Food | CLASS II | Coco's Italian Market Cannoli Making Kit recalledCoco's | Cocos Wholesale and Imports | Undeclared Milk | TN |
| Food | CLASS I | Strawberry Cream Cheese recalled by Made Fresh SaladsSalads | Made Fresh Salads | Listeria | NY |
| Food | CLASS II | Secondary Packaging: Steam Noodles Ingredients recalled by CNC NoodleSecondary Packaging | CNC Noodle | Undeclared Wheat & Gluten | CA, NV |
| Food | CLASS I | Scallion Cream Cheese recalled by Made Fresh SaladsSalads | Made Fresh Salads | Listeria | NY |
| Food | CLASS I | Lox Cream Cheese recalled by Made Fresh SaladsSalads | Made Fresh Salads | Listeria | NY |
| Food | CLASS I | 4893 Chicago Vanilla Naturally Flavored Ice Cream tub recalledHouse | House Of Flavors | Undeclared Egg | IL |
| Food | CLASS I | Whipped Cream Cheese recalled by Made Fresh SaladsSalads | Made Fresh Salads | Listeria | NY |
| Food | CLASS II | Frozen Raw Bulk Blueberry Crumble Pie ES (4 pies/case) recalled | Willamette Valley Pie Company | Listeria | IL, OR |
| Food | CLASS II | Lowes Foods sour cream and onion flavored potato chips recalledLowes | Uncle Ray's | Undeclared Allergens | NC |
| Food | HEALTH ALERT | Frozen Ready-To-Eat Turkey Stuffed Pastry Products recalled | Shaw Bakers | Labeling Errors | |
| Device | CLASS II | ShockPulse-SE Lithotripsy System Spl-s ShockPulse-SE recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS II | HiResolution Bionic Ear System Sky CI M90 Sound Processor recalled | Advanced Bionics | Packaging Defects | CA |
| Device | CLASS II | ShockPulse-SE Lithotripsy System - Reuseable Probes recalled | Olympus Corporation of the Americas | Other | PA |
| Device | CLASS II | Gelsoft Plus recalled by Vascutek | Vascutek | Labeling Errors | Nationwide |
| Device | CLASS II | STA Liatest Free Protein recalled by Diagnostica Stago | Diagnostica Stago | Device Malfunction | Nationwide |
| Device | CLASS II | ShockPulse-SE Lithotripsy System Spl-sr ShockPulse-SE recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS II | BBraun Medical Winged INF recalled | B Braun Medical | Device Malfunction | Nationwide |
| Device | CLASS II | B. Braun Winged Infusion, Single PK recalled by B Braun Medical | B Braun Medical | Device Malfunction | Nationwide |
| Device | CLASS II | CS100 IABP recalled by Datascope | Datascope | Device Malfunction | Nationwide |
| Device | CLASS II | Atellica CH Urine Albumin (UAlb) recalled | Siemens Healthcare Diagnostics | Other | Nationwide |
| Device | CLASS II | CS300 IABP recalled by Datascope | Datascope | Device Malfunction | Nationwide |
| Device | CLASS II | Centricity Universal Viewer Zero Footprint Client recalled | GE Healthcare | Device Malfunction | Nationwide |
| Device | CLASS II | cobas pro integrated solutions recalled by Roche Diagnostics Operations | Roche Diagnostics Operations | Potency & Assay | Nationwide |
| Device | CLASS II | Endocavity ultrasonic probe recalled by Esaote S.p.a | Esaote | Packaging Defects | Nationwide |
| Device | CLASS II | Minop Trocar 4 Wking Channel6 recalled by Aesculap | Aesculap | Device Malfunction | Nationwide |
| Device | CLASS II | EVO+ Visian Toric Implantable Collamer Lens (TICL) recalled | Staar Surgical | Other | N/A |
| Device | CLASS I | Impella RP recalled by Abiomed | Abiomed | Device Malfunction | Nationwide |
| Device | CLASS II | B. Braun Winged INF SET recalled by B Braun Medical | B Braun Medical | Device Malfunction | Nationwide |
| Device | CLASS II | ShockPulse-SE Lithotripsy System - Generator recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS I | Impella RP with SmartAssist recalled by Abiomed | Abiomed | Device Malfunction | Nationwide |
| Device | CLASS II | Olympus Single Use Biopsy Valve recalled by Olympus Corporation of the | Olympus Corporation of the Americas | Foreign Material | Nationwide |
| Device | CLASS I | Impella RP Flex with SmartAssist recalled by Abiomed | Abiomed | Device Malfunction | Nationwide |
| Device | CLASS II | Olympus Single use Biopsy Valve recalled by Olympus Corporation of the | Olympus Corporation of the Americas | Foreign Material | Nationwide |
| Drug | CLASS I | Silintan 25/pills recalled by ANTHONY TRINH, 123Herbals | Anthony Trinh 123Herbals | Labeling Errors | Nationwide |
| Drug | CLASS II | Children's Healthcare of Atlanta recalled by Acme United | Acme United | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Metoprolol Succinate Extended-Release Tablets recalledMetoprolol Succinate | Teva Pharmaceuticals USA | Potency & Assay | Nationwide |
| Drug | CLASS II | BZK Antiseptic Towelettes (Benzalkonium Chloride 0.13%) recalled | Acme United | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | WP WipesPlus Hand Sanitizing Wipes recalled by Acme United | Acme United | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Cleansing Towelette (Benzalkonium Chloride 0.13%) recalledMed Nap Cleansing Towelette | Acme United | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Metoprolol Succinate Extended-Release Tablets, 200 mg recalledMetoprolol Succinate | Teva Pharmaceuticals USA | Potency & Assay | Nationwide |
| Drug | CLASS II | Green Guard Antiseptic Wipes (Benzalkonium Chloride 0.13%) recalledGreen Guard Antiseptic Wipes | Acme United | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Metoprolol Succinate Extended-Release Tablets, 25 mg bottles recalledMetoprolol Succinate | Teva Pharmaceuticals USA | Potency & Assay | Nationwide |
| Drug | CLASS II | Sodium Iodide (I-131) Solution, Therapeutic Oral recalled by RadnostixSodium Iodide I-131 | Radnostix | Particulate Matter | Nationwide |
| Drug | CLASS II | Amnesteem (Isotretinoin) Capsules, USP 40 mg recalledAmnesteem | Mylan Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS I | MR. 7 Super blister card recalled by StuffbyNainax | StuffbyNainax | Labeling Errors | TX |
| Drug | CLASS III | Nilotinib Capsules recalled by Cipla USANilotinib | Cipla USA | Potency & Assay | Nationwide |
| Drug | CLASS II | Semaglutide, For Rx compounding use only recalled | Harbin Jixianglong Biotech | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Dukal BZK Antiseptic Towelette (Benzalkonium Chloride 0.13%) recalled | Acme United | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Medi-First Antiseptic Wipes recalled by Acme UnitedMedi-first Antiseptic Wipes | Acme United | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Max Packaging Antibacterial Towelette recalled by Acme United | Acme United | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Antimicrobial Alcohol Hand Wipe, Isopropyl Alcohol recalled | Acme United | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Metoprolol Succinate Extended-Release Tablets, 50 mg bottles recalledMetoprolol Succinate | Teva Pharmaceuticals USA | Potency & Assay | Nationwide |
| Drug | CLASS II | Dynarex, BZK Antiseptic Towelettes recalled by Acme UnitedBzk Pads | Acme United | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Semaglutide Inj, 2mg x 10, Sterile Multi-Dose Vial recalled | New Life Pharma | Sterility | OH |
| Drug | CLASS II | Tirzepatide Inj, 10mg, Sterile Multi-Dose Vial recalled | New Life Pharma | Sterility | OH |
| Drug | CLASS II | Dynarex Obstetrical Towelettes Cleanser recalled by Acme UnitedBzk Pads | Acme United | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | First Aid Only BZK Antiseptic Towelettes recalled by Acme UnitedFirst Aid Only Bzk Antiseptic | Acme United | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Maximum, Zone 1, 4% Lidocaine Cream recalled by HTO Nevada | HTO Nevada | Potency & Assay | Nationwide |
| Drug | CLASS II | Hand Sanitizing Wipes (Benzalkonium Chloride 0.13%) recalledFirst Aid Only Hand Sanitizing Wipe | Acme United | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | BZK Antiseptic Towelettes (Benzalkonium Chloride 0.13%) recalledMed Nap Benzalkonium Chloride Antiseptic | Acme United | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Tirzepatide Inj, 15mg x 4, Sterile Multi-Dose Vial recalled | New Life Pharma | Sterility | OH |
| Drug | CLASS I | Mojo Max Fusion XXX, 500 mg, one capsule per blister card recalled | Mohamed Hagar | Labeling Errors | Nationwide |
| Drug | CLASS II | Savannah Antibacterial Towelettes recalled by Acme United | Acme United | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Med-Nap Cleansing Towelettes (Benzalkonium Chloride 0.13%) recalledMed Nap Cleansing Towelette | Acme United | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Maximum, Zone 2, 4% Lidocaine Cream, (Lidocaine recalled by HTO Nevada | HTO Nevada | Potency & Assay | Nationwide |
| Drug | CLASS II | Five-star, Vasocaine Spray, (Lidocaine HCl recalled by HTO Nevada | HTO Nevada | Potency & Assay | Nationwide |
| Drug | CLASS II | First Aid Only BZK Antiseptic Towelettes recalled by Acme UnitedFirst Aid Only Bzk Antiseptic | Acme United | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Wipes Plus, Hand Sanitizing Alcohol Free BZK Wipes recalled | Acme United | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Semaglutide Inj., 2 mg x 5, Sterile Multi-Dose Vial recalled | New Life Pharma | Sterility | OH |
| Drug | CLASS II | First Aid Only BZK Antiseptic Towelette recalled by Acme UnitedFirst Aid Only Bzk Antiseptic | Acme United | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Product label: Temozolomide Capsules, 5mg recalledTemozolomide | Rising Pharma Holding | Potency & Assay | Nationwide |
| Drug | CLASS II | Semaglutide, For Rx compounding use only recalled | Harbin Jixianglong Biotech | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Midodrine Hydrochloride Tablets, USP, 5 mg ( blister packs) recalledMidodrine Hydrochloride | The Harvard Drug Group | Packaging Defects | Nationwide |
| Drug | CLASS II | Dynarex, BZK Antiseptic Towelettes recalled by Acme UnitedBzk Pads | Acme United | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Med Nap BZK Antiseptic Towelettes recalled by Acme UnitedMed Nap Benzalkonium Chloride Antiseptic | Acme United | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS III | Nilotinib Capsules recalled by Cipla USANilotinib | Cipla USA | Potency & Assay | Nationwide |
| Food | CLASS II | Premium Food Bubble Gum recalled by Bader Enterprises | Bader Enterprises | Undeclared Allergens | NJ, NY |
| Food | CLASS I | Lobster & Crab Ravioli recalled by Perfect Pasta, IncorporatedLobster | Perfect Pasta, Incorporated | Undeclared Fish & Shellfish | UT |
| Food | CLASS II | Premium Food Jordan Almonds recalled by Bader Enterprises | Bader Enterprises | Undeclared Allergens | NJ, NY |
| Food | CLASS I | Karns Foods, Mini Dark Chocolate Raspberry Cups Clear recalledKarns | Karns Prime And Fancy Foods | Undeclared Peanuts | PA |
| Food | CLASS II | Vergani 1944 Milano 'Pandoro Classico' Gluten Free recalledVergani | Italianway Import | Foreign Material | FL, MI, NJ |
| Food | CLASS I | Junebar Peanut Chocolate Chip All Natural Snack Bar recalledJunebar | Juniper Granola | Undeclared Milk | NY |
| Food | CLASS II | tippy toes apple pear banana 6 months & up baby food 2- Packs recalled | IF Holding II | Other | IL |
| Food | CLASS I | Junebar Chocolate Cherry All Natural Snack Bar recalledJunebar | Juniper Granola | Undeclared Milk | NY |
| Device | CLASS II | Adapt Pump recalled by Agiliti Health - Ellis | Agiliti Health - Ellis | Device Malfunction | Nationwide |
| Device | CLASS II | Medline Convenience Kits: NAIL KIT recalled by Medline Industries | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | PIE Trolley System recalled by Edermy | Edermy | Other | Nationwide |
| Device | CLASS II | Olympus Inner Sheath, Long recalled by Olympus Corporation of the | Olympus Corporation of the Americas | Device Malfunction | Nationwide |
| Device | CLASS II | Hitachi Proton Beam Therapy recalled by Hitachi, Ltd. Radiation | Hitachi, Ltd. Radiation Oncology Systems, Kashiwanoha | Device Malfunction | DC, TX |
| Device | CLASS II | Medline kits containing Tego Connectors Medline Apheresis recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | Olympus Inner Sheath recalled by Olympus Corporation of the | Olympus Corporation of the Americas | Device Malfunction | Nationwide |
| Device | CLASS II | Olympus Resection Sheath recalled by Olympus Corporation of the | Olympus Corporation of the Americas | Device Malfunction | Nationwide |
| Device | CLASS II | Medline Convenience Kits: Trunk KIT recalled by Medline Industries | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Medline Sterile Saline Wound Wash recalled by Medline Industries | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Empowr 3d Knee Ins, Ve recalled by Encore Medical | Encore Medical | Labeling Errors | Nationwide |
| Device | CLASS II | Olympus Cystoscope Outer Sheath recalled by Olympus Corporation of the | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS II | Olympus Resection Sheath recalled by Olympus Corporation of the | Olympus Corporation of the Americas | Device Malfunction | Nationwide |
| Device | CLASS II | Campy CVA Medium, R01272 recalled by Remel | Remel | Other Bacterial Contamination | Nationwide |
| Device | CLASS II | Olympus Resection Sheath recalled by Olympus Corporation of the | Olympus Corporation of the Americas | Device Malfunction | Nationwide |
| Device | CLASS II | Olympus Inner Sheath recalled by Olympus Corporation of the | Olympus Corporation of the Americas | Device Malfunction | Nationwide |
| Device | CLASS II | Olympus Resection Sheath recalled by Olympus Corporation of the | Olympus Corporation of the Americas | Device Malfunction | Nationwide |
| Device | CLASS II | PIE PAK recalled by Edermy | Edermy | Other | Nationwide |
| Device | CLASS II | Olympus Resection Inner Sheath recalled by Olympus Corporation of the | Olympus Corporation of the Americas | Device Malfunction | Nationwide |
| Device | CLASS II | Meijer Sterile saline wound wash, First Aid Cleansing Spray recalled | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Olympus Inner Sheath recalled by Olympus Corporation of the | Olympus Corporation of the Americas | Device Malfunction | Nationwide |
| Device | CLASS II | Hitachi Proton Beam Therapy System recalled by Hitachi, Ltd. Radiation | Hitachi, Ltd. Radiation Oncology Systems, Kashiwanoha | Device Malfunction | DC, TX |
| Device | CLASS II | Olympus Resection Sheath recalled by Olympus Corporation of the | Olympus Corporation of the Americas | Device Malfunction | Nationwide |
| Device | CLASS II | Reverse Shoulder Prosthesis recalled by Encore Medical | Encore Medical | Labeling Errors | Nationwide |
| Device | CLASS II | Olympus Resection Sheath recalled by Olympus Corporation of the | Olympus Corporation of the Americas | Device Malfunction | Nationwide |
| Device | CLASS II | Convenience kits containing Tego Connectors recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | Medline Kits containing Tego Connectors: Medline IR Pack recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | Medline Convenience Kits: NAIL KIT recalled by Medline Industries | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Olympus Resection Sheath recalled by Olympus Corporation of the | Olympus Corporation of the Americas | Device Malfunction | Nationwide |
| Device | CLASS II | Octopus Nuvo Tissue Stabilizer recalled by Medtronic Perfusion Systems | Medtronic Perfusion Systems | Other | Nationwide |
| Device | CLASS II | Olympus Resection Inner Sheath recalled by Olympus Corporation of the | Olympus Corporation of the Americas | Device Malfunction | Nationwide |
| Device | CLASS II | Olympus Inner Sheath recalled by Olympus Corporation of the | Olympus Corporation of the Americas | Device Malfunction | Nationwide |
| Device | CLASS II | Olympus Resection Sheath recalled by Olympus Corporation of the | Olympus Corporation of the Americas | Device Malfunction | Nationwide |
| Device | CLASS II | Olympus Inner Sheath recalled by Olympus Corporation of the | Olympus Corporation of the Americas | Device Malfunction | Nationwide |
| Device | CLASS II | Olympus Resection Sheath recalled by Olympus Corporation of the | Olympus Corporation of the Americas | Device Malfunction | Nationwide |
| Device | CLASS II | Convenience kits used for dialysis maintenance Medline Add recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | Olympus Inner Sheath, Long recalled by Olympus Corporation of the | Olympus Corporation of the Americas | Device Malfunction | Nationwide |
| Device | CLASS II | MRI LED Mobile Exam Light Battery recalled by MRIMed | MRIMed | Device Malfunction | Nationwide |
| Device | CLASS II | Olympus Resection Sheath., with Deflecting Obturator recalled | Olympus Corporation of the Americas | Device Malfunction | Nationwide |
| Device | CLASS II | Reverse Shoulder Prosthesis recalled by Encore Medical | Encore Medical | Labeling Errors | Nationwide |
| Device | CLASS II | Olympus Sheath recalled by Olympus Corporation of the | Olympus Corporation of the Americas | Device Malfunction | Nationwide |
| Device | CLASS II | Convenience kits containing Tego Connectors Medline recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | Medline Kits containing Tego Connectors Medline Dialysis ON/OFF KIT recalled | Medline Industries | Packaging Defects | Nationwide |
| Drug | CLASS II | CHNaO Fluorescein Sodium Ophthalmic Strips, USP 1mg, packaged as a) recalledC20h10na2o5 Fluorescein Sodium Ophthalmic Strips | Wizcure Pharmaa Private | Sterility | Nationwide |
| Drug | CLASS II | iKids-Growth (Day Formula) capsules recalled by Agebox | Agebox | Labeling Errors | Nationwide |
| Drug | CLASS II | Vista Meibo Tears Propylene Glycol 0.6% w/v Eye Drops recalledVista Meibo Tears Propylene Glycol 0.6% W/v Advanced Dry Eye Relief Lubricating Drops 10 Ml | Wizcure Pharmaa Private | Sterility | Nationwide |
| Drug | CLASS II | iKids-Growth (Night Formula), Manufactured Exclusively recalled | Agebox | Labeling Errors | Nationwide |
| Drug | CLASS II | Vista Gonio Eye Lubricant, Hypromellose Ophthalmic Solution recalledVista Gonio Eye Lubricant | Wizcure Pharmaa Private | Sterility | Nationwide |
| Drug | CLASS II | Adbry, (tralokinumab-ldrm) injection, 300 mg recalled by Leo PharmaAdbry | LEO Pharma | Particulate Matter | Nationwide |
| Drug | CLASS II | Vista Gel Hypromellose USP 0.3% w/v recalled by Wizcure Pharmaa PrivateVista Hypromellose Dry Eye Relief | Wizcure Pharmaa Private | Sterility | Nationwide |
| Drug | CLASS II | Amantadine HCl, Capsules, UPS, 100 mg dose recalled by AvKAREAmantadine Hcl | AvKARE | Potency & Assay | Nationwide |
| Drug | CLASS III | Eptifibatide Injection, 75 mg/ vial recalledEptifibatide | Slate Run Pharmaceuticals | Other | Nationwide |
| Drug | CLASS II | Vista Tears Polyethylene Glycol 400 0.4% w/v recalled | Wizcure Pharmaa Private | Sterility | Nationwide |
| Drug | CLASS II | Bio Glo Fluorescein Sodium Ophthalmic Strips recalled | Wizcure Pharmaa Private | Sterility | Nationwide |
| Drug | CLASS II | BioGlo Fluorescein Sodium Ophthalmic Strips recalled | Wizcure Pharmaa Private | Sterility | Nationwide |
| Food | CLASS I | Dried Croaker Fish recalled by Prime Food ProcessingPrime | Prime Food Processing | Other | 18 states |
| Food | CLASS III | Mung Beans recalled by Lubna Quality ProductsMung | Lubna Quality Products | Packaging Defects | LA, TX |
| Food | CLASS II | Valley Springs 100% Natural Bottled Water recalledValley Springs | Valley Springs Artesian Gold | Foreign Material | IL, WI |
| Food | CLASS I | IQF frozen Blueberry cases and totes) recalled by Oregon Potato CompanyIqf | Oregon Potato Company | Listeria | 4 states |
| Food | CLASS II | Yoyo Gummy Assorted Flavor recalled by Sb FoodYoyo Gummy | Sb Food | Foreign Material | 15 states |
| Food | CLASS II | Gerber Arrowroot Biscuits recalledGerber Arrowroot | Gerber Products | Foreign Material | Nationwide |
| Food | CLASS II | Yoyo Gummy Tropical Flavor recalled by Sb FoodYoyo Gummy | Sb Food | Foreign Material | 15 states |
| Food | CLASS II | Tiki Bar Candy Dark Chocolatey Peanut Butter & Pretzel recalledTiki | J2C Hawaii | Undeclared Peanuts | HI |
| Food | CLASS II | Valley Springs Steamed Distilled Water recalledValley Springs | Valley Springs Artesian Gold | Other | IL, WI |
| Food | CLASS II | Yoyo Gummy Grape Plus Flavor recalled by Sb FoodYoyo Gummy | Sb Food | Foreign Material | 15 states |
| Food | CLASS I | Fish Ball, Frozen per pack Wt recalled by Min Jiang Food Store | Min Jiang Food Store | Undeclared Allergens | 8 states |
| Food | CLASS II | Wellsley Farms Farm- Raised Atlantic Salmon recalledWellsley | Slade Gorton & Co | Listeria | MD |
| Food | CLASS I | Organics Organic Chia Seeds recalled by NavitasNavitas Organics | Navitas | Salmonella | 26 states |
| Food | CLASS I | Fish Ball, Frozen per pack Wt recalled by Min Jiang Food Store | Min Jiang Food Store | Undeclared Allergens | 8 states |
| Food | CLASS III | Yo!man Lettuce (spicy Flavor) recalled by Tengen Usa Trading | Tengen Usa Trading | Undeclared Allergens | 5 states |
| Food | CLASS III | Yo!man Cucumber (fresh Hunan Flavor) recalled by Tengen Usa Trading | Tengen Usa Trading | Undeclared Allergens | 5 states |
| Food | CLASS II | Valley Springs 100% Natural Bottled Water recalledValley Springs | Valley Springs Artesian Gold | Other | IL, WI |
| Food | CLASS I | Fish Ball, Frozen per pack Wt recalled by Min Jiang Food Store | Min Jiang Food Store | Undeclared Allergens | 8 states |
| Food | CLASS I | For Chicken and Pork Fried Rice, Ramen, and Shu Mai Products recalled | Ajinomoto Foods North America, Ajinomoto Toyo Frozen Noodle, Inc., Ajinomoto Foods North America | Foreign Material | |
| Food | HEALTH ALERT | Ready-To-Eat Beef Jerky Products recalled by Punahele Jerky | Punahele Jerky | Undeclared Soy | |