| Device | CLASS II | Equinoxe Ergo Adjustable Angle rTSA Reamer recalled by Exactech | Exactech | Device Malfunction | SC |
| Device | CLASS II | Medline convenience kits labeled as: Basic Neuro Pack recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Medline convenience kits labeled as: Head And Neck recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Medline convenience kits labeled as: Gyn Laparotomy Harper Pack-lf recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | A clear, plastic capillary blood collection tube coated with Heparin recalled | ASP Global | Foreign Material | Nationwide |
| Device | CLASS II | The Safe-t-fill Capillary Blood Collection System recalled by ASP Global | ASP Global | Other | Nationwide |
| Device | CLASS II | Medline convenience kits labeled as: Port Insertion Pack recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | PhD Hemostasis Valve recalled by Merit Medical Systems | Merit Medical Systems | Packaging Defects | 50 states |
| Device | CLASS II | The Safe-t-fill Capillary Blood Collection System recalled by ASP Global | ASP Global | Other | Nationwide |
| Device | CLASS II | Medline convenience kits labeled as: Breast Biopsy Pack-lf recalled | Medline Industries | E. coli | Nationwide |
| Device | CLASS II | Safe-t-fill Micro Collection Tube Extender recalled by ASP Global | ASP Global | Other | Nationwide |
| Device | CLASS II | Reprocessed Imaging Catheter Acuson recalled by Sterilmed | Sterilmed | Sterility | 8 states |
| Device | CLASS II | Medline Sterile Basic Eye Pack recalled by Medline Industries | Medline Industries | Sterility | MO |
| Device | CLASS II | Medline convenience kits labeled as: Minor Single Basin Pack recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Mosaiq Oncology Information System recalled by Elekta Solutions Ab | Elekta Solutions AB | Device Malfunction | Nationwide |
| Device | CLASS II | Medline convenience kits labeled as: General Laparoscopy recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Equinoxe Ergo Augments Pilot Tip Converter recalled by Exactech | Exactech | Device Malfunction | SC |
| Device | CLASS II | A clear, plastic capillary blood collection tube recalled by ASP Global | ASP Global | Foreign Material | Nationwide |
| Device | CLASS II | HeartMate 3 Left Ventricular System (LVAS) Kits recalled by Thoratec | Thoratec | Device Malfunction | Nationwide |
| Device | CLASS II | Monarch Bronchoscope recalled by Auris Health | Auris Health | Packaging Defects | Nationwide |
| Device | CLASS II | Medline convenience kits labeled as: General Aaa #11-RF recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | A clear, plastic capillary blood collection tube recalled by ASP Global | ASP Global | Foreign Material | Nationwide |
| Device | CLASS II | The Safe-t-fill Capillary Blood Collection System recalled by ASP Global | ASP Global | Other | Nationwide |
| Device | CLASS II | Medline convenience kits labeled as: Major Laparotomy Cds recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Medline convenience kits labeled as Local Basic recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Catheter Acunav Diagnostic Ultrasound Not For Use recalled by Sterilmed | Sterilmed | Sterility | 8 states |
| Device | CLASS II | HeartMate II¿ LVAS Implant Kit recalled by Thoratec | Thoratec | Device Malfunction | Nationwide |
| Device | CLASS II | DxFLEX Flow Cytometer recalled by Beckman Coulter | Beckman Coulter | Device Malfunction | Nationwide |
| Device | CLASS II | Tribio Implant recalled by Berkeley Advanced Biomaterials | Berkeley Advanced Biomaterials | Packaging Defects | Nationwide |
| Device | CLASS II | The Safe-t-fill Capillary Blood Collection System recalled by ASP Global | ASP Global | Other | Nationwide |
| Device | CLASS II | Safe-t-fill Magnetic Rings for Safe-t-fill Blood Gas Capillaries recalled | ASP Global | Other | Nationwide |
| Device | CLASS II | BD Luer Tip Caps recalled by Becton Dickinson & | Becton Dickinson | Other | Nationwide |
| Device | CLASS II | Medline convenience kits labeled as: Cath Lab Pacemaker Pack recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | ReQuest Measles IgG Rubeola IgG Enzyme Linked Immunoabsorbant Assay recalled | Quest International | Potency & Assay | UT, WA |
| Device | CLASS II | A clear, plastic capillary blood collection tube coated with Heparin recalled | ASP Global | Foreign Material | Nationwide |
| Device | CLASS II | Medline convenience kits labeled as: C-section OR 30 Cds recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | The Safe-t-fill Capillary Blood Collection System recalled by ASP Global | ASP Global | Other | Nationwide |
| Device | CLASS II | HeartMate II¿ Controller (standalone) recalled by Thoratec | Thoratec | Device Malfunction | Nationwide |
| Device | CLASS I | TMJ Bilateral Implant recalled by TMJ Solutions | TMJ Solutions | Other | 15 states |
| Device | CLASS II | Vacuette CAT Serum Separator Clot Activator recalled | Greiner Bio-One North America | Potency & Assay | 28 states |
| Device | CLASS II | A clear, plastic capillary blood collection tube recalled by ASP Global | ASP Global | Foreign Material | Nationwide |
| Device | CLASS II | MC3 VitalFlow Console recalled by Medtronic Perfusion Systems | Medtronic Perfusion Systems | Other | Nationwide |
| Device | CLASS II | Group B Streptococcus recalled by Meridian Bioscience | Meridian Bioscience | Foreign Material | 14 states |
| Device | CLASS II | Medline convenience kits labeled as: Major Vaginal Harper Pack-lf recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | The Safe-t-fill Capillary Blood Collection System recalled by ASP Global | ASP Global | Other | Nationwide |
| Device | CLASS II | Mixing Fleas for Safe-t-fill Blood Gas Capillaries recalled | ASP Global | Other | Nationwide |
| Device | CLASS II | A clear, plastic capillary blood collection tube recalled by ASP Global | ASP Global | Foreign Material | Nationwide |
| Device | CLASS II | Medline convenience kits labeled as: Gyn Laparoscopy Cds #34-RF recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Olympus Nephro-EZDilate Nephrostomy Balloon Catheter recalled | Olympus Corporation of the Americas | Packaging Defects | 6 states |
| Device | CLASS III | OC-Auto Fobt-chek Negative Controls is the negative recalled | Polymedco, Inc. / Polymedco Cancer Diagnostic Products | Labeling Errors | 47 states |
| Device | CLASS II | Medtronic Hr-act (High Range Activated Clotting Time Cartridges) recalled | Medtronic Perfusion Systems | Other | Nationwide |
| Device | CLASS II | The Safe-t-fill Capillary Blood Collection System recalled by ASP Global | ASP Global | Other | Nationwide |
| Device | CLASS II | alethia c. Difficile recalled by Meridian Bioscience | Meridian Bioscience | Foreign Material | 14 states |
| Device | CLASS II | The Safe-t-fill Capillary Blood Collection System recalled by ASP Global | ASP Global | Other | Nationwide |
| Device | CLASS II | Equinoxe Ergo Adjustable Angle rTSA Reamer recalled by Exactech | Exactech | Device Malfunction | SC |
| Device | CLASS II | A clear, plastic capillary blood collection tube recalled by ASP Global | ASP Global | Foreign Material | Nationwide |
| Device | CLASS II | HeartMate 3 Controller (Standalone) recalled by Thoratec | Thoratec | Device Malfunction | Nationwide |
| Device | CLASS I | BD Alaris infusion Pump Module recalled by CareFusion 303 | CareFusion 303 | Device Malfunction | Nationwide |
| Device | CLASS II | Medline convenience kits labeled as: Gp-leep Pack-lf recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Medline convenience kits labeled as: Central Line Pack recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | A clear, plastic capillary blood collection tube recalled by ASP Global | ASP Global | Foreign Material | Nationwide |
| Device | CLASS II | Medline convenience kits labeled as: Minor Eye Tray #81 recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | REF: CC286297 or BS737162 Automated Digital Cell Morphology analyzer recalled | Cellavision AB | Other | Nationwide |
| Device | CLASS II | The Safe-t-fill Capillary Blood Collection System recalled by ASP Global | ASP Global | Other | Nationwide |
| Device | CLASS II | Medline convenience kits labeled as: Circumcision Pack recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | A clear, plastic capillary blood collection tube recalled by ASP Global | ASP Global | Foreign Material | Nationwide |
| Device | CLASS II | The Safe-t-fill Capillary Blood Collection System recalled by ASP Global | ASP Global | Other | Nationwide |
| Device | CLASS II | The Safe-t-fill Capillary Blood Collection System recalled by ASP Global | ASP Global | Other | Nationwide |
| Device | CLASS II | A clear, plastic capillary blood collection tube recalled by ASP Global | ASP Global | Foreign Material | Nationwide |
| Device | CLASS II | Medline convenience kits labeled as: Ach Plastics Breast-lf recalled | Medline Industries | E. coli | Nationwide |
| Drug | CLASS II | DermaCerin, Skin Protectant Moisturizing Cream (petrolatum 33%) recalled | DermaRite Industries | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS III | Fesoterodine Fumarate, Extended-release Tablets, 4 mg recalledFesoterodine Fumarate | Alembic Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS II | 4-N-1 Skin Protectant, No Rinse Wash Cream recalled | DermaRite Industries | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS III | Klarity-C Drops (Cyclosporine) recalled by Imprimis NJOF | Imprimis Njof | Potency & Assay | Nationwide |
| Drug | CLASS II | McKesson Skin Protectant, Lanolin recalled by DermaRite IndustriesSkin Protectant With Lanolin | DermaRite Industries | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Bromocriptine Mesylate Capsules, USP, 5 mg recalledBromocriptine Mesylate | Zydus Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS II | Lantiseptic, Dry Skin Therapy, Lanolin recalled by DermaRite Industries | DermaRite Industries | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Renew Skin Repair Cream, Dimethicone recalled by DermaRite Industries | DermaRite Industries | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Fentanyl citrate, 2 mcg / ml / Ropivacaine, 0.2% in NS, CII recalled | Park Avenue Compounding | Manufacturing (CGMP) Deviations | MO |
| Drug | CLASS I | Potassium Chloride Inj., 20 mEq total in Flexible Container recalledPotassium Chloride | Otsuka ICU Medical | Other | Nationwide |
| Drug | CLASS II | Hand-E-Foam, Benzethonium Chloride recalled by DermaRite Industries | DermaRite Industries | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | GelRite Instant Hand Sanitizer, Alcohol recalled by DermaRite Industries | DermaRite Industries | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | UltraSure Anti-Perspirant & Deodorant recalled by DermaRite Industries | DermaRite Industries | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS I | Potassium Chloride Inj., 10 mEq total in Flexible Container recalledPotassium Chloride | Otsuka ICU Medical | Other | Nationwide |
| Drug | CLASS II | San-E-Foam, Alcohol 67% per cartridge recalled by DermaRite Industries | DermaRite Industries | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | DermaKleen, Health Care Antiseptic Lotion Soap recalled | DermaRite Industries | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Niacin Extended-Release Tablets, USP, 1,000 mg recalledNiacin | Golden State Medical Supply | Potency & Assay | Nationwide |
| Drug | CLASS II | Renew PeriProtect, Zinc Oxide 12%, Dimethicone 1% per tube recalled | DermaRite Industries | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | PeriGuard Ointment, Petrolatum recalled by DermaRite Industries | DermaRite Industries | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | DermaMed Ointment, Skin Protectant, Aluminum Hydroxide Gel recalled | DermaRite Industries | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | PeriGiene, Health Care Antiseptic, Chloroxylenol recalled | DermaRite Industries | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | DermaSarra, Camphor 0.5%, External Analgesic recalled | DermaRite Industries | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | DermaFungal, Antifungal Cream with 2% Miconazole Nitrate recalled | DermaRite Industries | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | KleenFoam Antimicrobial Foam Soap recalled by DermaRite Industries | DermaRite Industries | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Lantiseptic, Skin Protectant, Lanolin recalled by DermaRite Industries | DermaRite Industries | Manufacturing (CGMP) Deviations | Nationwide |
| Food | CLASS I | Peppercorn cheese round cheese wheel, made with raw milk recalledTwin Sisters | Twin Sisters Creamery | E. coli | OR, WA |
| Food | CLASS I | Item# 28855 Whatcom Blue, Twin Sisters Creamery products recalledItem | Peterson Company | E. coli | 4 states |
| Food | CLASS I | Rockport Lobser Bisque recalled by Plenus GroupRockport Lobser | Plenus Group | Undeclared Fish & Shellfish | 10 states |
| Food | CLASS II | Cinnamon Powder recalled by HaitaiCinnamon | Haitai | Lead & Heavy Metals | Nationwide |
| Food | CLASS I | Farmhouse Cheese round cheese wheel, made with raw milk recalledTwin Sisters | Twin Sisters Creamery | E. coli | OR, WA |
| Food | CLASS I | Mustard Seed cheese round cheese wheel, made recalledTwin Sisters | Twin Sisters Creamery | E. coli | OR, WA |
| Food | CLASS I | Publix Rich & Creamy Vanilla Ice Cream recalled by Publix Super MarketsPublix Rich | Publix Super Markets | Undeclared Egg | 4 states |
| Food | CLASS I | Organic Moringa Powder recalled by Bulk & OrganicBulk | Bulk & Organic | Salmonella | CA, NJ, NY |
| Food | CLASS I | Dry Ghoinnya Fish recalled by New Hoque and SonsDry Ghoinnya | New Hoque and Sons | Other | NJ, NY |
| Food | CLASS I | Item# 29608 Farmhouse White, Twin Sisters Creamery products recalledItem | Peterson Company | E. coli | 4 states |
| Food | CLASS I | Whatcom Blue cheese round cheese wheel, made recalledTwin Sisters | Twin Sisters Creamery | E. coli | OR, WA |
| Device | CLASS I | Anesthesia circuit kit recalled by Medline Industries | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | NutraGlide, 5 f - 6F x 55 Nasal Feeding Tube with Stylet and ENfit recalled | Applied Medical Technology | Other | Nationwide |
| Device | CLASS II | DigitalDiagnost 4 High Performance, Flex/Value recalled | Philips Medical Systems DMC | Other | Nationwide |
| Device | CLASS II | Harmonic Focus Shears + Adaptive Tissue Technology Length recalled | Stryker Sustainability Solutions | Other | Nationwide |
| Device | CLASS II | Medline Renewal LigaSure Maryland Jaw Sealer/Divider Nano recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS I | Magnetom Cima.X Upgrade recalled by Siemens Medical Solutions USA | Siemens Medical Solutions USA | Packaging Defects | CA |
| Device | CLASS II | Medline Renewal LigaSure Maryland Jaw Sealer/Divider recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | Ceiling Type X-Ray Tube Support recalled by Shimadzu Corporation Medical | Shimadzu Corporation Medical Systems Division | Device Malfunction | Nationwide |
| Device | CLASS II | Single Use Electrosurgical Snare recalled by Olympus Corporation of the | Olympus Corporation of the Americas | Sterility | Nationwide |
| Device | CLASS II | BD Kiestra" Isolate Suspension Cuvette Array recalled | Becton Dickinson | Other | Nationwide |
| Device | CLASS II | Medline Renewal LigaSure Impact Curved Large Jaw recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS I | Convenience kits recalled by Medline Industries | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | Medline Renewal LigaSure Exact recalled by Medline Industries | Medline Industries | Other | Nationwide |
| Device | CLASS II | Virata Preassembled Polyaxial Screw, utilized recalled by Orthofix U.S | Orthofix U.S | Other | Nationwide |
| Device | CLASS II | BEAR Implant (Bridge-Enhanced ACL Restoration) recalled | Miach Orthopaedics | Other | Nationwide |
| Device | CLASS II | GM85 Digital Mobile X-ray imaging System recalled by NeuroLogica | NeuroLogica | Foreign Material | Nationwide |
| Device | CLASS II | Brand Name: Sonesta Product Name: 6210 Model/Catalog Number recalled | Sonesta Medical AB | Device Malfunction | NH |
| Device | CLASS II | Carescape B450 recalled by GE Healthcare Finland Oy | GE Healthcare Finland Oy | Device Malfunction | Nationwide |
| Device | CLASS I | Anesthesia Circuit Kits and other various kits that contain recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS I | Convenience Kits: DYNJ901048N Ortho Spine ST Clair recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | CombiDiagnost R90 recalled by Philips Medical Systems DMC | Philips Medical Systems DMC | Other | Nationwide |
| Device | CLASS II | Immulite 2000 Oak Mix Specific Allergen recalled | Siemens Healthcare Diagnostics | Labeling Errors | Nationwide |
| Device | CLASS I | Convenience kits recalled by Medline Industries | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | Battery Flex-3S2P 10.8V 18650 Li-ion Smbus used recalled | GE Healthcare Finland Oy | Device Malfunction | Nationwide |
| Device | CLASS II | Medline RenewalLigasure Blunt Tip Sealer/Divider recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | Alinity hq Analyzer recalled by Abbott Laboratories | Abbott Laboratories | Device Malfunction | Nationwide |
| Device | CLASS II | ProxiDiagnost N90 recalled by Philips Medical Systems DMC | Philips Medical Systems DMC | Other | Nationwide |
| Device | CLASS I | Convenience Kit, Breast Hernia DYNJ909125G recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | 3gAllergy Specific IgE Universal Kit recalled | Siemens Healthcare Diagnostics | Labeling Errors | Nationwide |
| Device | CLASS II | NutraGlide, 5 F- 6 F x 55 Nasal Feeding Tube with Stylet and ENfit recalled | Applied Medical Technology | Other | Nationwide |
| Device | CLASS I | Anesthesia Circuit Kits and other various kits that contain recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | Single Use Single Use Electrosurgical Snare recalled | Olympus Corporation of the Americas | Sterility | Nationwide |
| Device | CLASS II | Signia" Small Diameter Curved Tip Intelligent Reload Vascular/Thin) recalled | Covidien | Other | Nationwide |
| Device | CLASS II | NutraGlide, 5 F- 6 F x 90 Nasal Feeding Tube with Stylet and ENfit recalled | Applied Medical Technology | Other | Nationwide |
| Device | CLASS II | NutraGlide, 6 F- 8 F x 55 Nasal Feeding Tube with Stylet and ENfit recalled | Applied Medical Technology | Other | Nationwide |
| Device | CLASS I | Dynj909119g Robotic Gastric Lap Sleeve-lf Dynj909127f Cysto recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS I | Anesthesia Circuit Kits and other various kits that contain recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | Medline Renewal Ligasure Blunt Tip Sealer/Divider recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | Liberta RC DBS IPG (Implantable Pulse Generator) recalled | Abbott Medical | Other | TX |
| Device | CLASS II | Multichem ID recalled by Techno-path Manufacturing | Techno-path Manufacturing | Potency & Assay | 17 states |
| Device | CLASS III | VerifyNow PRUTest Platelet Reactivity Test recalled | Accriva Diagnostics | Packaging Defects | Nationwide |
| Device | CLASS II | Food Panel 3 Specific Allergen recalled | Siemens Healthcare Diagnostics | Labeling Errors | Nationwide |
| Device | CLASS II | SimplyGo Mini, Standard Battery Kit recalled by Philips Respironics | Philips Respironics | Temperature Abuse | Nationwide |
| Device | CLASS I | Anesthesia Circuit Kits and other various kits that contain recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS I | Cerepak Detachable Coil System - Name recalled by Cerenovus | Cerenovus | Device Malfunction | Nationwide |
| Device | CLASS II | Medline Renewal Ligasure Maryland Jaw Sealer/Divider recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | Precision CRF recalled by Philips Medical Systems DMC | Philips Medical Systems DMC | Other | Nationwide |
| Device | CLASS II | Medline Renewal Ligasure Blunt Tip Sealer/Divider recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | Medline Renewal LigaSure Small Jaw Instrument recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | DigitalDiagnost C90 High Performance, Flex/Value/Chest/ER recalled | Philips Medical Systems DMC | Other | Nationwide |
| Device | CLASS II | Medline Renewal Ligasure Impact Sealer/Divider NanoCoated recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | Signia" Small Diameter Curved Tip Intelligent Reload Vascular/Thin) recalled | Covidien | Other | Nationwide |
| Device | CLASS II | Medline Renewal LigaSure Blunt Tip Sealer/Divider recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | Multichem ID recalled by Techno-path Manufacturing | Techno-path Manufacturing | Potency & Assay | 17 states |
| Device | CLASS II | Radiography recalled by Philips Medical Systems DMC | Philips Medical Systems DMC | Other | Nationwide |
| Device | CLASS II | Lithotriptor, Ultrasonic ShockPulse Lithotripsy Transducer recalled | Olympus Corporation of the Americas | Temperature Abuse | Nationwide |
| Device | CLASS II | NutraGlide, 6 F- 8 F x 90 Nasal Feeding Tube with Stylet and ENfit recalled | Applied Medical Technology | Other | Nationwide |
| Device | CLASS II | Affinity NT Oxygenator, Oxygenator recalled | Medtronic Perfusion Systems | Other | AZ, CA, TN |
| Food | CLASS I | Monarch Premium Kratom Bali Gold powder recalledMonarch | Lotus Vaping Technologies | Salmonella | Nationwide |
| Food | CLASS I | Monarch Premium Kratom Red Bali powder recalledMonarch | Lotus Vaping Technologies | Salmonella | Nationwide |
| Food | CLASS I | Carton Label: Pacific Fresh Vegetables Pacific recalledCarton Label | Pacific International Marketing | Salmonella | 8 states |
| Food | CLASS I | Lo-boy Foods recalled by Made Fresh SaladsLo-boy | Made Fresh Salads | Listeria | NY |
| Food | CLASS II | Tense-X. Package: 175cc HDPE recalled by Professional BotanicalsProduct Name | Professional Botanicals | Packaging Defects | Nationwide |
| Food | CLASS I | Zingerman's Ca$hew Cow Candy Bar recalled by Zingerman's CoffeeZingerman's Ca | Zingerman's Coffee | Undeclared Peanuts | MI, NY |
| Food | CLASS II | Loaded Veggie Grain Bowl recalled by FreshRealmLoaded Veggie | FreshRealm | Listeria | 11 states |
| Food | CLASS II | Roshni Cinnamon Powder recalled by Singh TradingRoshni Cinnamon | Singh Trading | Lead & Heavy Metals | 5 states |
| Food | CLASS I | Monarch Premium Kratom White Elephant powder recalledMonarch | Lotus Vaping Technologies | Salmonella | Nationwide |
| Food | CLASS I | Monarch Premium Kratom Green Maeng Da powder recalledMonarch | Lotus Vaping Technologies | Salmonella | Nationwide |
| Food | CLASS II | Blue Oven Artisan Bakery English Muffins recalled | Blue Oven Bakery | Undeclared Allergens | IN, KY, OH |
| Food | CLASS I | Zingerman's Peanut Butter Crush Candy Bar recalled by Zingerman's CoffeeZingerman's | Zingerman's Coffee | Undeclared Tree Nuts | MI, NY |
| Food | CLASS I | Carton Label: Pacific Fresh Vegetables Pacific recalledCarton Label | Pacific International Marketing | Salmonella | 8 states |
| Food | CLASS I | Lo-boy Foods recalled by Made Fresh SaladsLo-boy | Made Fresh Salads | Listeria | NY |
| Food | CLASS I | Carton Label: Pacific Straight From The Fields Fresh Herbs recalledCarton Label | Pacific International Marketing | Salmonella | 8 states |
| Food | CLASS II | Total Comfort recalled by Professional BotanicalsProduct Name | Professional Botanicals | Packaging Defects | Nationwide |
| Food | CLASS I | Peach Salsa recalled by GBC Food ServicesPeach | GBC Food Services | Listeria | 10 states |
| Food | CLASS II | Nutra Calm Package: 175cc HDPE recalled by Professional BotanicalsProduct Name | Professional Botanicals | Packaging Defects | Nationwide |
| Food | CLASS I | Peach Salsa - $5.99 recalled by Jfe FranchisingPeach | Jfe Franchising | Listeria | 18 states |
| Food | CLASS II | Mai California Roll WR recalled by Hana GroupMai California | Hana Group | Undeclared Allergens | 7 states |
| Food | CLASS I | Carton Label: Pacific Fresh Vegetables Pacific recalledCarton Label | Pacific International Marketing | Salmonella | 8 states |
| Food | CLASS I | Item IL1014A, Piggy Lotte Crispy Crunch Ice Cream Cone, Strawberry recalledItem IL1014A | Seoul Trading | Undeclared Peanuts | OR, WA |
| Device | CLASS II | TruDi¿ Navigation System - Multi Instrument Adapter recalled | Integra LifeSciences Corp. (NeuroSciences) | Device Malfunction | Nationwide |
| Device | CLASS II | Synchron Systems Direct Ldl Cholesterol (Ldld) Reagent recalled | Beckman Coulter | Other | Nationwide |
| Device | CLASS II | UniCel DxI 800, Part Numbers: 973100, A71456 recalled by Beckman Coulter | Beckman Coulter | Device Malfunction | MN |
| Device | CLASS I | Tandem Mobi Insulin Pump: Description recalled by Tandem Diabetes Care | Tandem Diabetes Care | Device Malfunction | 52 states |
| Device | CLASS I | Codman Disposable Perforator Cranial Perforator recalled | Integra LifeSciences Corp. (NeuroSciences) | Other | Nationwide |
| Device | CLASS II | Leksell Stereotactic System Leksell Vantage Stereotactic System recalled | Elekta | Device Malfunction | Nationwide |
| Device | CLASS II | bk3500 Ultrasound System w/battery recalled by B-K Medical A/S | B-K Medical | Device Malfunction | Nationwide |
| Device | CLASS II | Mahurkar" Acute High Pressure Triple Lumen Catheter Tray recalled | Mozarc Medical US | Packaging Defects | Nationwide |
| Device | CLASS II | Mahurkar" Acute High Pressure Triple Lumen Catheter Tray recalled | Mozarc Medical US | Packaging Defects | Nationwide |
| Device | CLASS II | Sentinel V11 recalled by Spacelabs Healthcare | Spacelabs Healthcare | Device Malfunction | Nationwide |
| Device | CLASS II | Osstem Dental X-Ray System T2Plus recalled by OSSTEM Implant Co | Osstem Implant | Other | N/A |
| Device | CLASS II | bk3000 Ultrasound System w/battery recalled by B-K Medical A/S | B-K Medical | Device Malfunction | Nationwide |
| Device | CLASS II | Mahurkar" Acute High Pressure Triple Lumen Catheter Tray recalled | Mozarc Medical US | Packaging Defects | Nationwide |
| Device | CLASS II | 1202 Flex Focus Ultrasound System, cart recalled by B-K Medical A/S | B-K Medical | Device Malfunction | Nationwide |
| Device | CLASS II | Klassic BiPolar Head recalled by Total Joint Orthopedics | Total Joint Orthopedics | Sterility | Nationwide |
| Device | CLASS II | Biomet Dual Mobility Vivacit-E Highly Crosslinked recalled by Zimmer | Zimmer | Packaging Defects | 20 states |
| Device | CLASS II | Osstem Dental X-Ray System T1 recalled by OSSTEM Implant Co | Osstem Implant | Other | N/A |
| Device | CLASS II | UUltrasound System 2300, bkActiv w/battery recalled by B-K Medical A/S | B-K Medical | Device Malfunction | Nationwide |
| Device | CLASS II | UniCel DxI 600, Part Numbers: A71460, A30260 recalled by Beckman Coulter | Beckman Coulter | Device Malfunction | MN |
| Device | CLASS II | Mahurkar" Acute High Pressure Triple Lumen Catheter Tray recalled | Mozarc Medical US | Packaging Defects | Nationwide |
| Device | CLASS II | bk5000 Ultrasound System w/battery recalled by B-K Medical A/S | B-K Medical | Device Malfunction | Nationwide |
| Device | CLASS II | Biomet Dual Mobility Vivacit-E Highly Crosslinked recalled by Zimmer | Zimmer | Packaging Defects | 20 states |
| Device | CLASS II | Osstem Dental X-Ray System T2 recalled by OSSTEM Implant Co | Osstem Implant | Other | N/A |
| Device | CLASS II | Ultrasound System 1300, bkSpecto w/battery recalled by B-K Medical A/S | B-K Medical | Device Malfunction | Nationwide |
| Device | CLASS II | Mahurkar" Acute High Pressure Triple Lumen Catheter Tray recalled | Mozarc Medical US | Packaging Defects | Nationwide |
| Device | CLASS I | Codman Disposable Perforator Cranial Perforator recalled | Integra LifeSciences Corp. (NeuroSciences) | Other | Nationwide |
| Device | CLASS II | Mahurkar" Acute High Pressure Triple Lumen Catheter Tray recalled | Mozarc Medical US | Packaging Defects | Nationwide |
| Device | CLASS II | Inclusive Titanium Screw compatible with: Biomet 3i" Certain recalled | Prismatik Dentalcraft | Packaging Defects | 18 states |
| Drug | CLASS II | clomiPRAMINE Hydrochloride, Capsules, USP, 75 mg recalledClomipramine Hydrochloride | Zydus Pharmaceuticals | Nitrosamine Impurity | Nationwide |
| Drug | CLASS II | clomiPRAMINE Hydrochloride, Capsules, USP, 50 mg recalledClomipramine Hydrochloride | Zydus Pharmaceuticals | Nitrosamine Impurity | Nationwide |
| Drug | CLASS II | clomiPRAMINE Hydrochloride, Capsules, USP, 25 mg recalledClomipramine Hydrochloride | Zydus Pharmaceuticals | Nitrosamine Impurity | Nationwide |
| Drug | CLASS II | Acetaminophen 500mg Caffeine 65mg caplets recalled by Aero HealthcareAerotab Pain Reliever | Aero Healthcare | Packaging Defects | Nationwide |
| Drug | CLASS II | Amoxicillin and Clavulanate Potassium recalled | Teva Pharmaceuticals USA | Potency & Assay | CA, MS, OH |
| Food | CLASS II | Best Yet Frozen Raw EZ-Peel White Shrimp 16/20 recalledBest Yet | Admiralty Island Fisheries | Other | Nationwide |
| Food | CLASS I | Big Y Brown Jumbo A Eggs recalled by Eggs UnlimitedBig Y | Eggs Unlimited | Salmonella | CA, CT, OR |
| Food | CLASS II | Strawberry Cheesecake Ice Cream recalled by Ice Cream Factory | Ice Cream Factory | Foreign Material | 29 states |
| Food | CLASS I | Giant/Martin's Crunchy Taco Dinner Kit recalled by Teasdale FoodsGiant | Teasdale Foods | Undeclared Allergens | 11 states |
| Food | CLASS II | Frozen Coconut bar recalled by Que Rikura's Products | Que Rikura's Products | Undeclared Sulfites | FL |
| Food | CLASS II | Kroger Raw Colossal EZ Peel Shrimp recalledKroger | Admiralty Island Fisheries | Packaging Defects | Nationwide |
| Food | CLASS I | In-shell chicken eggs distributed on Jacob King's farm recalledIn-shell | Jacob King | Salmonella | NY |
| Food | CLASS II | AquaStar Raw Peeled Tail-on Shrimp Skewers recalledAquaStar | Admiralty Island Fisheries | Packaging Defects | Nationwide |
| Food | CLASS I | Pastured Grade AA Large Eggs " recalled by Kenz Henz | Kenz Henz | Salmonella | TX |
| Food | CLASS II | Publix Extra Large Shrimp Easy to Peel Deveined 21/25 recalledPublix Extra | Admiralty Island Fisheries | Other | Nationwide |
| Food | CLASS II | Publix Large Shrimp Peeled & Deveined Tail On 31/40 recalledPublix | Admiralty Island Fisheries | Other | Nationwide |
| Food | CLASS II | Bakery Graham Pieces Label reads recalled by Ice Cream Factory | Ice Cream Factory | Foreign Material | 29 states |
| Food | CLASS II | AquaStar 13/15 Raw Shrimp Easy Peel Deveined recalledAquaStar | Admiralty Island Fisheries | Other | Nationwide |
| Food | CLASS I | Casa Mamita Soft Taco Dinner Kit recalled by Teasdale FoodsCasa Mamita | Teasdale Foods | Undeclared Allergens | 11 states |
| Food | CLASS II | Dr. Praeger's, California Veggie Burgers recalledDr. Praeger's | Dr. Praeger's Sensible Foods | Listeria | FL, NJ, NY |
| Food | CLASS II | Eagle Spice Ground Ginger recalledEagle | Eagle Spice and Extract Co | Lead & Heavy Metals | 4 states |
| Food | CLASS II | Specialty Stuft Meats Crawfish Stuft Potato recalledSpecialty Stuft | Quality Poultry & Seafood | Undeclared Allergens | AL, LA, MS |
| Food | CLASS II | Waterfront Bistro Frozen Raw EZ-Peel White Shrimp 21/25 recalledWaterfront Bistro | Admiralty Island Fisheries | Other | Nationwide |
| Food | CLASS I | Frozen Crab Paste recalled by New York Mutual Trading | New York Mutual Trading | Undeclared Allergens | 7 states |
| Food | CLASS II | Lucky Foods Cinnamon Powder recalled by TBC Distribution CorporateLucky | TBC Distribution Corporate | Lead & Heavy Metals | 11 states |
| Food | CLASS II | AquaStar 16/20 Frozen Raw EZ-Peel White Shrimp recalledAquaStar | Admiralty Island Fisheries | Other | Nationwide |
| Food | CLASS II | Kroger Mercado Cooked Medium Peeled Tail-Off Shrimp recalledKroger Mercado | Admiralty Island Fisheries | Foreign Material | Nationwide |
| Device | CLASS II | Various models of BD Pyxis Medbank: Reference numbers recalled | CareFusion 303 | Other | Nationwide |
| Device | CLASS II | All Serial Numbers/BD Pyxis CII Safe ES Tower Main, REF recalled | CareFusion 303 | Other | Nationwide |
| Device | CLASS II | Alcon Laboratories, Inc Accessory devices for Unity recalled | Alcon Research | Sterility | Nationwide |
| Device | CLASS II | Refill 18 Coated Regular and 18 Coated Super Tampons recalled | Daye (Anne's DAY Ltd) | Other | Nationwide |
| Device | CLASS II | 9 Coated Regular Tampons and 9 Nude Regular Tampons recalled | Daye (Anne's DAY Ltd) | Other | Nationwide |
| Device | CLASS II | Initiation 18 Coated Super and 18 Nude Super Tampons recalled | Daye (Anne's DAY Ltd) | Other | Nationwide |
| Device | CLASS II | Sealing Unit For Trocars recalled by Aesculap | Aesculap | Packaging Defects | Nationwide |
| Device | CLASS II | Sealing Cap For Trocars recalled by Aesculap | Aesculap | Packaging Defects | Nationwide |
| Device | CLASS II | 9 Coated Regular and 9 Coated Super Tampons recalled | Daye (Anne's DAY Ltd) | Other | Nationwide |
| Device | CLASS II | All in One Bundle recalled by Daye (anne's Day Ltd) | Daye (Anne's DAY Ltd) | Other | Nationwide |
| Device | CLASS II | ChemoLock Universal Vented Vial Spike recalled by ICU Medical | ICU Medical | Packaging Defects | Nationwide |
| Device | CLASS II | The Endomag Magseed Pro Magnetic Marker System is a sterile recalled | Endomagnetics | Other | Nationwide |
| Device | CLASS II | ChemoLock Vented Vial Spike recalled by ICU Medical | ICU Medical | Packaging Defects | Nationwide |
| Device | CLASS II | 60" Appx, Ext Set, Smallbore w/ChemoLock Port, Clamp recalled | ICU Medical | Packaging Defects | Nationwide |
| Device | CLASS I | Imris Operating Suite, iMRI 3T recalled by IMPRIS Imaging | Impris Imaging | Packaging Defects | Nationwide |
| Device | CLASS II | In Vitro Diagnostic external control recalled by Microgenics | Microgenics | Potency & Assay | Nationwide |
| Device | CLASS II | ChemoLock Bag Spike recalled by ICU Medical | ICU Medical | Packaging Defects | Nationwide |
| Device | CLASS II | Refill 3 Month Trial Tampon recalled by Daye (anne's Day Ltd) | Daye (Anne's DAY Ltd) | Other | Nationwide |
| Device | CLASS II | ChemoLock Vented Vial Spike recalled by ICU Medical | ICU Medical | Packaging Defects | Nationwide |
| Device | CLASS II | Refill 36 Coated Regular Tampons recalled by Daye (anne's Day Ltd) | Daye (Anne's DAY Ltd) | Other | Nationwide |
| Device | CLASS II | Assay: Immulite 2000 Intact PTH recalled | Siemens Healthcare Diagnostics | Potency & Assay | Nationwide |
| Device | CLASS II | Alcon Laboratories, Inc Accessory devices for Unity recalled | Alcon Research | Sterility | Nationwide |
| Device | CLASS II | ChemoLock Bag Spike with Clave Additive Port recalled by ICU Medical | ICU Medical | Packaging Defects | Nationwide |
| Device | CLASS II | 9 Coated Regular and 9 Nude Regular Tampons recalled | Daye (Anne's DAY Ltd) | Other | Nationwide |
| Device | CLASS II | Sharesource Connectivity Platform for Use with Homechoice Claria recalled | Vantive US Healthcare | Device Malfunction | Nationwide |
| Device | CLASS II | Regular Flow Bundle recalled by Daye (anne's Day Ltd) | Daye (Anne's DAY Ltd) | Other | Nationwide |
| Device | CLASS II | 7.5" Appx, Ext Set w/ChemoLock" Port, Clamp, Graduated Adapter recalled | ICU Medical | Packaging Defects | Nationwide |
| Device | CLASS II | 18 Coated Super Tampons recalled by Daye (anne's Day Ltd) | Daye (Anne's DAY Ltd) | Other | Nationwide |
| Device | CLASS II | Oncology Kit w/31" 20 Drop Admin Set w/Integrated recalled | ICU Medical | Packaging Defects | Nationwide |
| Device | CLASS II | ChemoLock w/Mini Bag Spike ¿ recalled by ICU Medical | ICU Medical | Packaging Defects | Nationwide |
| Device | CLASS II | SyncAR Surgical Navigation Advanced Platform Patient recalled | Surgical Theater | Device Malfunction | Nationwide |
| Device | CLASS II | Initiation 18 Coated Regular and 18 Nude Regular Tampons recalled | Daye (Anne's DAY Ltd) | Other | Nationwide |
| Device | CLASS II | Xpert SA Nasal Complete recalled by Cepheid | Cepheid | Potency & Assay | Nationwide |
| Device | CLASS II | Initiation 18 Coated Regular and 18 Coated Super Tampons recalled | Daye (Anne's DAY Ltd) | Other | Nationwide |
| Device | CLASS II | Greiner Bio-one Vacuette 9NC Coagulation sodium citrate recalled | Greiner Bio-One North America | Other | Nationwide |
| Device | CLASS I | Imris Operating Suite, Imris iMRI 3T recalled by IMPRIS Imaging | Impris Imaging | Packaging Defects | Nationwide |
| Device | CLASS II | 73" Appx, Ext Set, Smallbore w/ChemoLock Port, Clamp recalled | ICU Medical | Packaging Defects | Nationwide |
| Device | CLASS II | Initiation 3 Month Heavy Flow Bundle recalled by Daye (anne's Day Ltd) | Daye (Anne's DAY Ltd) | Other | Nationwide |
| Device | CLASS II | 6" Ext Set w/MicroClave" Clear, ChemoLock" Port recalled by ICU Medical | ICU Medical | Packaging Defects | Nationwide |
| Device | CLASS II | ChemoLock Closed Vial Spike recalled by ICU Medical | ICU Medical | Packaging Defects | Nationwide |
| Device | CLASS II | Refill 36 Coated Super Tampons recalled by Daye (anne's Day Ltd) | Daye (Anne's DAY Ltd) | Other | Nationwide |
| Device | CLASS II | 31" Appx, Admin Set w/20 Drop Integrated ChemoLock Drip recalled | ICU Medical | Packaging Defects | Nationwide |
| Device | CLASS II | 8" Ext Set w/MicroClave Clear, ChemoLock Port, Y-Connector recalled | ICU Medical | Packaging Defects | Nationwide |
| Device | CLASS II | Surgical Navigation Advanced Platform Patient Engagement (PE SNAP) recalled | Surgical Theater | Device Malfunction | Nationwide |
| Device | CLASS II | Ivenix Infusion System (IIS), Large Volume Pump recalled | Fresenius Kabi USA | Other | Nationwide |
| Device | CLASS II | Refill 3 Month Heavy Flow Bundle recalled by Daye (anne's Day Ltd) | Daye (Anne's DAY Ltd) | Other | Nationwide |
| Device | CLASS II | Refill 18 Coated Super and 18 Nude Super Tampons recalled | Daye (Anne's DAY Ltd) | Other | Nationwide |
| Device | CLASS II | MST ArcDUO recalled by MicroSurgical Technology | MicroSurgical Technology | Other | Nationwide |
| Device | CLASS II | ChemoLock Closed Vial Spike recalled by ICU Medical | ICU Medical | Packaging Defects | Nationwide |
| Device | CLASS II | Various models of BD Pyxis Pro 7-Drawer Auxiliary, Reference numbers recalled | CareFusion 303 | Other | Nationwide |
| Device | CLASS II | Heavy Flow Bundle recalled by Daye (anne's Day Ltd) | Daye (Anne's DAY Ltd) | Other | Nationwide |
| Device | CLASS II | Initiation 3 Month Regular Flow Bundle recalled by Daye (anne's Day Ltd) | Daye (Anne's DAY Ltd) | Other | Nationwide |
| Device | CLASS I | G6 Continuous Glucose Monitoring System Dexcom G6 recalled | Dexcom | Device Malfunction | Nationwide |
| Device | CLASS II | Oncology Kit w/ChemoLock, ChemoLock Port recalled by ICU Medical | ICU Medical | Packaging Defects | Nationwide |
| Device | CLASS II | Trial Tampon recalled by Daye (anne's Day Ltd) | Daye (Anne's DAY Ltd) | Other | Nationwide |
| Device | CLASS II | Surgical Navigation Advanced Platform (SNAP) recalled | Surgical Theater | Device Malfunction | Nationwide |
| Device | CLASS II | Alcon Laboratories, Inc Accessory devices for Unity recalled | Alcon Research | Sterility | Nationwide |
| Device | CLASS II | Initiation 36 Coated Super Tampons recalled by Daye (anne's Day Ltd) | Daye (Anne's DAY Ltd) | Other | Nationwide |
| Device | CLASS II | ChemoLock Bag Spike recalled by ICU Medical | ICU Medical | Packaging Defects | Nationwide |
| Device | CLASS II | Model: Incisive CT; Product Code (REF): (1) 728143, (2) recalled | Philips Medical Systems | Device Malfunction | 18 states |
| Device | CLASS II | 45" Appx, Smallbore Ext Set w/Spiros w/Red Cap recalled by ICU Medical | ICU Medical | Packaging Defects | Nationwide |
| Device | CLASS II | Initiation 3 Month All in One Bundle recalled by Daye (anne's Day Ltd) | Daye (Anne's DAY Ltd) | Other | Nationwide |
| Device | CLASS II | ChemosafeLock Bag Spike recalled by ICU Medical | ICU Medical | Packaging Defects | Nationwide |
| Device | CLASS II | Alcon Laboratories, Inc Accessory devices for Unity recalled | Alcon Research | Sterility | Nationwide |
| Device | CLASS II | Double ChemoLock Port Syringe Transfer Set recalled by ICU Medical | ICU Medical | Packaging Defects | Nationwide |
| Device | CLASS II | Oncology Kit w/2 ChemoLock" Closed Vial Spike w/ChemoLock" recalled | ICU Medical | Packaging Defects | Nationwide |
| Device | CLASS II | ChemoLock Port recalled by ICU Medical | ICU Medical | Packaging Defects | Nationwide |
| Device | CLASS I | MEGA Ballast Distal Access Platform Mega Ballast recalled by Balt Usa | Balt USA | Device Malfunction | 12 states |
| Device | CLASS II | Safe-t-fill Micro Capillary Blood Collection recalled by ASP Global | ASP Global | Foreign Material | Nationwide |
| Device | CLASS II | Various models of BD Pyxis MedFlex, Reference numbers recalled | CareFusion 303 | Other | Nationwide |
| Device | CLASS II | Clave Bag Spike w/ChemoLock Port recalled by ICU Medical | ICU Medical | Packaging Defects | Nationwide |
| Device | CLASS II | Graduated Connector w/ChemoLock Port recalled by ICU Medical | ICU Medical | Packaging Defects | Nationwide |
| Device | CLASS II | ChemoLock Vial Spike recalled by ICU Medical | ICU Medical | Packaging Defects | Nationwide |
| Device | CLASS II | Medistim MiraQ System recalled by Medistim A | Medistim Asa | Device Malfunction | 5 states |
| Device | CLASS II | Reducing Converter recalled by Aesculap | Aesculap | Packaging Defects | Nationwide |
| Device | CLASS II | SpineAR Surgical Navigation Advanced Platform Patient recalled | Surgical Theater | Device Malfunction | Nationwide |
| Device | CLASS II | 30" Appx, 20 Drop Admin Set w/Integrated ChemoLock Port recalled | ICU Medical | Packaging Defects | Nationwide |
| Device | CLASS II | Endo Surgical Navigation Advanced Platform Patient recalled | Surgical Theater | Device Malfunction | Nationwide |
| Device | CLASS II | Oncology Transfer Kit w/ChemoClave and ChemoLock Port recalled | ICU Medical | Packaging Defects | Nationwide |
| Device | CLASS II | Good Neighbor Pharmacy, True Metrix Self Monitoring Blood recalled | Trividia Health | Device Malfunction | Nationwide |
| Device | CLASS II | Sealing Unit F/ Trocars W.reducer recalled by Aesculap | Aesculap | Packaging Defects | Nationwide |
| Device | CLASS II | CellMek SPS Sample Preparation System recalled by Beckman Coulter | Beckman Coulter | Device Malfunction | Nationwide |
| Device | CLASS II | Model: CT 5300; Product Code (REF): 728285; Software Versions recalled | Philips Medical Systems | Device Malfunction | 18 states |
| Device | CLASS II | Surgical Planner, BrainSTORM recalled by Surgical Theater | Surgical Theater | Device Malfunction | Nationwide |
| Device | CLASS II | SuRgical Planner (SRP) recalled by Surgical Theater | Surgical Theater | Device Malfunction | Nationwide |
| Device | CLASS II | ChemosafeLock Vial Adapter REFs recalled by ICU Medical | ICU Medical | Packaging Defects | Nationwide |
| Device | CLASS II | Initiation 3 Month Trial Tampon recalled by Daye (anne's Day Ltd) | Daye (Anne's DAY Ltd) | Other | Nationwide |
| Device | CLASS II | 30" Appx, Admin Set w/20 Drop Integrated ChemoLock Drip recalled | ICU Medical | Packaging Defects | Nationwide |
| Device | CLASS II | 6.5" Bag Spike w/ChemoLock Port Additive Port, ChemoLock Port recalled | ICU Medical | Packaging Defects | Nationwide |
| Device | CLASS II | Vantage Galan 3t recalled by Canon Medical System, USA | Canon Medical System USA | Other | NV, OH |
| Device | CLASS II | 9 Coated Super and 9 Nude Super Tampons recalled | Daye (Anne's DAY Ltd) | Other | Nationwide |
| Device | CLASS II | Initiation 36 Coated Regular Tampons recalled by Daye (anne's Day Ltd) | Daye (Anne's DAY Ltd) | Other | Nationwide |
| Device | CLASS II | 21" Ext Set w/ChemoLock Port, Clamp, Graduated Connector recalled | ICU Medical | Packaging Defects | Nationwide |
| Device | CLASS II | Chemo Lock Universal Vented Vial Spike recalled by ICU Medical | ICU Medical | Packaging Defects | Nationwide |
| Device | CLASS II | ChemoLock Vented Vial Spike ¿ recalled by ICU Medical | ICU Medical | Packaging Defects | Nationwide |
| Device | CLASS II | Syringe Transfer Set w/MicroClave, ChemoLock Port recalled | ICU Medical | Packaging Defects | Nationwide |
| Device | CLASS II | ChemosafeLock Connecter recalled by ICU Medical | ICU Medical | Packaging Defects | Nationwide |
| Device | CLASS II | The Endomag Magseed Pro Magnetic Marker System is a sterile recalled | Endomagnetics | Other | Nationwide |
| Device | CLASS II | BD Pyxis Pro MedStation Main recalled by CareFusion 303 | CareFusion 303 | Other | Nationwide |
| Device | CLASS II | Alcon Laboratories, Inc Accessory devices for Unity recalled | Alcon Research | Sterility | Nationwide |
| Device | CLASS II | ChemoLock" Port, Bulk, Non-Sterile recalled by ICU Medical | ICU Medical | Packaging Defects | Nationwide |
| Device | CLASS I | Imris Operating Suite, InVision 3T Operating Suite recalled | Impris Imaging | Packaging Defects | Nationwide |
| Device | CLASS II | ChemoLock Port w/Spiros, Red Cap recalled by ICU Medical | ICU Medical | Packaging Defects | Nationwide |
| Device | CLASS II | 18 Coated Regular Tampons recalled by Daye (anne's Day Ltd) | Daye (Anne's DAY Ltd) | Other | Nationwide |
| Device | CLASS II | Refill 3 Month Regular Flow Bundle recalled by Daye (anne's Day Ltd) | Daye (Anne's DAY Ltd) | Other | Nationwide |
| Device | CLASS II | 9 Coated Super Tampons and 9 Nude Super Tampons recalled | Daye (Anne's DAY Ltd) | Other | Nationwide |
| Device | CLASS II | Refill 18 Coated Regular and 18 Nude Regular Tampons recalled | Daye (Anne's DAY Ltd) | Other | Nationwide |
| Device | CLASS II | ChemoLock Closed Vial Spike w/Skirt recalled by ICU Medical | ICU Medical | Packaging Defects | Nationwide |
| Device | CLASS II | Refill 3 Month All in One Bundle recalled by Daye (anne's Day Ltd) | Daye (Anne's DAY Ltd) | Other | Nationwide |
| Device | CLASS I | Imris Operating Suite, Neuro Iii-sv iMRI System recalled | Impris Imaging | Packaging Defects | Nationwide |
| Device | CLASS II | Model: Incisive CT for Brazil SKD; Product Code (REF) recalled | Philips Medical Systems | Device Malfunction | 18 states |
| Device | CLASS II | Alcon PRECISION1 One-Day Contact Lenses, -2.25D recalled | Alcon Research | Sterility | 19 states |
| Drug | CLASS II | Desipramine Hydrochloride Tablets, USP, 75 mg bottle recalledDesipramine Hydrochloride | Heritage Pharmaceuticals | Nitrosamine Impurity | Nationwide |
| Drug | CLASS II | Lisdexamfetamine Dimesylate Capsules, 30 mg, CII recalledLisdexamfetamine Dimesylate | SUN Pharmaceutical Industries | Potency & Assay | Nationwide |
| Drug | CLASS III | Everolimus tablets 5mg (each carton contains 4 blister recalled | Endo USA | Potency & Assay | Nationwide |
| Drug | CLASS II | Testosterone 87.5 MG, 1 Pellet (Sterile) For Subcutaneous Insertion recalled | Farmakeio Outsourcing | Particulate Matter | Nationwide |
| Drug | CLASS II | Lisdexamfetamine Dimesylate Capsules, 40 mg, CII recalledLisdexamfetamine Dimesylate | SUN Pharmaceutical Industries | Potency & Assay | Nationwide |
| Drug | CLASS III | Everolimus tablets 10 mg (each carton contains 4 blister recalled | Endo USA | Potency & Assay | Nationwide |
| Drug | CLASS II | Duloxetine Delayed-Release Capsules, USP, 60 mg, a.) bottle recalledDuloxetine | Breckenridge Pharmaceutical | Nitrosamine Impurity | Nationwide |
| Drug | CLASS II | Lisdexamfetamine Dimesylate Capsules, 10 mg, CII recalledLisdexamfetamine Dimesylate | SUN Pharmaceutical Industries | Potency & Assay | Nationwide |
| Drug | CLASS II | Prazosin Hydrochloride, Capsules, USP, 5 mg recalledPrazosin Hydrochloride | Teva Pharmaceuticals USA | Nitrosamine Impurity | Nationwide |
| Drug | CLASS II | Testosterone Regular Release 200 MG, 1 Pellet recalled | Farmakeio Outsourcing | Particulate Matter | Nationwide |
| Drug | CLASS II | Lisdexamfetamine Dimesylate Capsules, 20 mg, CII recalledLisdexamfetamine Dimesylate | SUN Pharmaceutical Industries | Potency & Assay | Nationwide |
| Drug | CLASS II | R.E.C.K. (Ropivacaine HCl, EPINEPHrine, CloNIDine HCl recalled | QuVa Pharma | Particulate Matter | Nationwide |
| Drug | CLASS II | Testosterone / Triamcinolone Acetonide, 62.5MG/12.5MCG recalled | Farmakeio Outsourcing | Particulate Matter | Nationwide |
| Drug | CLASS II | Desipramine Hydrochloride Tablets, USP, 100 mg bottle recalledDesipramine Hydrochloride | Heritage Pharmaceuticals | Nitrosamine Impurity | Nationwide |
| Drug | CLASS II | Desipramine Hydrochloride Tablets, USP, 50 mg bottle recalledDesipramine Hydrochloride | Heritage Pharmaceuticals | Nitrosamine Impurity | Nationwide |
| Drug | CLASS II | Testosterone 200 MG, 1 Pellet (Sterile) For Subcutaneous Insertion recalled | Farmakeio Outsourcing | Particulate Matter | Nationwide |
| Drug | CLASS II | Prazosin Hydrochloride, Capsules, USP, 1 mg recalledPrazosin Hydrochloride | Amerisource Health Services | Nitrosamine Impurity | Nationwide |
| Drug | CLASS II | Sting Relief Swabs, First Aid Only, 10 Swabs recalled by Acme United | Acme United | Packaging Defects | Nationwide |
| Drug | CLASS II | Lisdexamfetamine Dimesylate Capsules, 70 mg, CII recalledLisdexamfetamine Dimesylate | SUN Pharmaceutical Industries | Potency & Assay | Nationwide |
| Drug | CLASS II | Desipramine Hydrochloride Tablets, USP, 10 mg bottle recalledDesipramine Hydrochloride | Heritage Pharmaceuticals | Nitrosamine Impurity | Nationwide |
| Drug | CLASS II | Testosterone / Triamcinolone Acetonide 50MG/10MCG, 1 Pellet recalled | Farmakeio Outsourcing | Particulate Matter | Nationwide |
| Drug | CLASS II | Testosterone Regular Release 50 MG, 1 Pellet recalled | Farmakeio Outsourcing | Particulate Matter | Nationwide |
| Drug | CLASS II | Testosterone / Triamcinolone Acetonide 87.5MG/17.5MCG recalled | Farmakeio Outsourcing | Particulate Matter | Nationwide |
| Drug | CLASS II | Testosterone / Triamcinolone Acetonide Pellet (200MG/40MCG) recalled | Farmakeio Outsourcing | Particulate Matter | Nationwide |
| Drug | CLASS II | Prazosin Hydrochloride, Capsules, USP, 2 mg recalledPrazosin Hydrochloride | Amerisource Health Services | Nitrosamine Impurity | Nationwide |
| Drug | CLASS II | Testosterone 25MG, 1 Pellet (Sterile) For Subcutaneous Insertion recalled | Farmakeio Outsourcing | Particulate Matter | Nationwide |
| Drug | CLASS II | 0.9% Sodium Chloride Injection recalled by Otsuka ICU MedicalSodium Chloride | Otsuka ICU Medical | Sterility | Nationwide |
| Drug | CLASS II | Semaglutide Injection, 5 mg/ (2.5 mg/mL) Multidose Vial recalled | ProRx | Sterility | TX, UT |
| Drug | CLASS II | Testosterone / Triamcinolone Acetonide Pellet recalled | Farmakeio Outsourcing | Particulate Matter | Nationwide |
| Drug | CLASS III | Everolimus tablets 2.5 mg (each carton contains 4 blister recalled | Endo USA | Potency & Assay | Nationwide |
| Drug | CLASS II | Testosterone / Triamcinolone Acetonide, 12.5MG/2.5MCG recalled | Farmakeio Outsourcing | Particulate Matter | Nationwide |
| Drug | CLASS II | Semaglutide Injection (2.5 mg/mL) Multidose Vial recalled by ProRx | ProRx | Sterility | TX, UT |
| Drug | CLASS II | Prazosin Hydrochloride, Capsules, USP, 5 mg recalledPrazosin Hydrochloride | Amerisource Health Services | Nitrosamine Impurity | Nationwide |
| Drug | CLASS II | Lisdexamfetamine Dimesylate Capsules, 50 mg, CII recalledLisdexamfetamine Dimesylate | SUN Pharmaceutical Industries | Potency & Assay | Nationwide |
| Drug | CLASS II | Tylenol, Acetaminophen, Extra Strength, 24 Caplets, 500mg each recalledTylenol Extra Strength | Kenvue Brands | Other | Nationwide |
| Drug | CLASS II | Desipramine Hydrochloride Tablets, USP, 150 mg bottle recalledDesipramine Hydrochloride | Heritage Pharmaceuticals | Nitrosamine Impurity | Nationwide |
| Drug | CLASS II | Testosterone / Triamcinolone Acetonide Pellet (100MG/20MCG) recalled | Farmakeio Outsourcing | Particulate Matter | Nationwide |
| Drug | CLASS II | Tirzepatide Injection, 27 mg/ (9 mg/mL) Multidose Vial recalled by ProRx | ProRx | Sterility | TX, UT |
| Drug | CLASS II | Hadlima (adalimumab-bwwd) injection recalled by Samsung Bioepis Co | Samsung Bioepis | Sterility | NJ |
| Drug | CLASS II | Semaglutide Injection, 8mg/ (2.5 mg/mL) Multidose Vial recalled by ProRx | ProRx | Sterility | TX, UT |
| Drug | CLASS III | Everolimus tablets 7.5mg (each carton contains 4 blister recalled | Endo USA | Potency & Assay | Nationwide |
| Drug | CLASS III | Espumil, Lipophilic foam base, 24G15-T02 recalled by Letco Medical | Letco Medical | Other | AL |
| Drug | CLASS II | Testosterone 62.5 MG, 1 Pellet (Sterile) For Subcutaneous Insertion recalled | Farmakeio Outsourcing | Particulate Matter | Nationwide |
| Drug | CLASS II | Desipramine Hydrochloride Tablets, USP, 25 mg bottle recalledDesipramine Hydrochloride | Heritage Pharmaceuticals | Nitrosamine Impurity | Nationwide |
| Drug | CLASS II | Testosterone 50MG, 1 Pellet (Sterile) For Subcutaneous Insertion recalled | Farmakeio Outsourcing | Particulate Matter | Nationwide |
| Drug | CLASS II | Prazosin Hydrochloride, Capsules, USP, 1 mg recalledPrazosin Hydrochloride | Teva Pharmaceuticals USA | Nitrosamine Impurity | Nationwide |
| Drug | CLASS II | Lisdexamfetamine Dimesylate Capsules, 60 mg, CII recalledLisdexamfetamine Dimesylate | SUN Pharmaceutical Industries | Potency & Assay | Nationwide |
| Drug | CLASS II | Semaglutide Injection, 2.5mg/ (2.5 mg/mL) Multidose Vial recalled | ProRx | Sterility | TX, UT |
| Drug | CLASS II | Prazosin Hydrochloride, Capsules, USP, 2 mg recalledPrazosin Hydrochloride | Teva Pharmaceuticals USA | Nitrosamine Impurity | Nationwide |
| Drug | CLASS II | Testosterone / Triamcinolone Acetonide 25MG/5MCG, 1 Pellet recalled | Farmakeio Outsourcing | Particulate Matter | Nationwide |
| Drug | CLASS II | Semaglutide Injection, 6mg/ (2.5 mg/mL) Multidose Vial recalled by ProRx | ProRx | Sterility | TX, UT |
| Drug | CLASS II | Semaglutide Injection, 10 mg/ (2.5 mg/mL) Multidose Vial recalled | ProRx | Sterility | TX, UT |
| Food | CLASS II | Mixed Nuts Roasted No Salt recalled by Severn Peanut Company | Severn Peanut Company | Undeclared Tree Nuts | MA, NY |
| Food | CLASS II | CaBOT Creamery Sea Salt Caramel Cheddar Sweet & Cheesy recalledCaBOT | Jody's | Undeclared Peanuts | IL |
| Food | CLASS II | Deli Express BBQ Pulled Pork on a sesame bun recalled by E.A. SweenDeli Express | E.A. Sween | Foreign Material | Nationwide |
| Food | CLASS II | Mixed Nuts Roasted & Salted recalled by Severn Peanut Company | Severn Peanut Company | Undeclared Tree Nuts | MA, NY |
| Food | CLASS II | Riced Cauliflower Iqf recalled by Nate's Fine FoodsRiced Cauliflower | Nate's Fine Foods | Listeria | IN, TX |
| Food | CLASS I | 47518 - Nonpareil, Semi-Sweet Chocolate recalled by Weaver Nut Company | Weaver Nut Company | Undeclared Milk | 14 states |
| Food | CLASS II | Marketside Cheesy Cauliflower Au Gratin recalled by FreshRealmMarketside Cheesy | FreshRealm | Listeria | IN |
| Food | CLASS I | EchoLakeFoods MF 3067 Cnfree Cage Free Precooked IAF Scrambled Eggs recalledEchoLakeFoods MF | Echo Lake Foods | Listeria | CA |
| Food | CLASS I | D2645 - Nonpareils, Semi-Sweet Chocolate recalled by Weaver Nut CompanyD2645 | Weaver Nut Company | Undeclared Milk | 14 states |
| Food | CLASS I | Carrot Bundt Cake recalled by Doan's Dessert And Coffee | Doan's Dessert And Coffee | Undeclared Allergens | Nationwide |
| Food | CLASS I | White Chocolate Coconut Bundt Cake recalled by Doan's Dessert And Coffee | Doan's Dessert And Coffee | Undeclared Allergens | Nationwide |
| Food | CLASS I | Fusia Asian Inspirations Veggie Spring Rolls recalled by Tai Foong USAAsian Inspirations | Tai Foong USA | Undeclared Fish & Shellfish | 23 states |
| Food | CLASS I | Frozen Chicken and Beef Croquette Products recalled by Brazilian Taste | Brazilian Taste | Undeclared Sesame | |