| Food | ANNOUNCED | 365 Whole Foods Market Standardized + Full Spectrum Blend recalled365 Whole Foods Market | Vitality Works | Salmonella | 31 states |
| Food | ANNOUNCED | Wise Wife Ground cinnamon recalled by SLR Food DistributionWise Wife | SLR Food Distribution | Lead & Heavy Metals | 14 states |
| Food | CLASS II | Honey Nut Granola recalled by El Ruisenor De Mexico | El Ruisenor De Mexico | Undeclared Allergens | 7 states |
| Food | CLASS III | Chocolate Covered Almonds recalled by El Ruisenor De Mexico | El Ruisenor De Mexico | Undeclared Allergens | 7 states |
| Food | CLASS III | Jovy Watermelon Gummy Rings recalled by El Ruisenor De MexicoJovy Watermelon | El Ruisenor De Mexico | Undeclared Allergens | 7 states |
| Food | CLASS I | Homestyle Poblano Mole recalled by El Ruisenor De MexicoHomestyle Poblano | El Ruisenor De Mexico | Undeclared Sulfites | 7 states |
| Food | CLASS III | Dried Whole Shrimp recalled by El Ruisenor De Mexico | El Ruisenor De Mexico | Undeclared Allergens | 7 states |
| Food | CLASS II | Apple Rings recalled by El Ruisenor De Mexico | El Ruisenor De Mexico | Undeclared Sulfites | 7 states |
| Food | CLASS III | Hazelnuts in Shell recalled by El Ruisenor De MexicoHazelnuts | El Ruisenor De Mexico | Undeclared Allergens | 7 states |
| Food | CLASS II | Andronico's Community Markets 100% Squeezed Orange recalledAndronico's Community | Voila Juice | Other | CA |
| Food | CLASS III | Tube Shaped Wheat Snack recalled by El Ruisenor De Mexico | El Ruisenor De Mexico | Undeclared Allergens | 7 states |
| Food | CLASS III | Walnuts in Shell recalled by El Ruisenor De MexicoWalnuts | El Ruisenor De Mexico | Undeclared Allergens | 7 states |
| Food | CLASS II | Roasted & Salted Mixed Nuts recalled by El Ruisenor De Mexico | El Ruisenor De Mexico | Undeclared Allergens | 7 states |
| Food | CLASS II | Dried Diced Papaya recalled by El Ruisenor De Mexico | El Ruisenor De Mexico | Undeclared Sulfites | 7 states |
| Food | CLASS II | Fritura Rueda / Wheat Wheel Snack recalled by El Ruisenor De MexicoFritura Rueda | El Ruisenor De Mexico | Undeclared Allergens | 7 states |
| Food | CLASS II | Dried Papaya Spears recalled by El Ruisenor De Mexico | El Ruisenor De Mexico | Undeclared Sulfites | 7 states |
| Food | CLASS III | Whole Wheat recalled by El Ruisenor De Mexico | El Ruisenor De Mexico | Undeclared Allergens | 7 states |
| Food | CLASS II | Jovy Gummy Worms (Regular) recalled by El Ruisenor De MexicoJovy Gummy | El Ruisenor De Mexico | Undeclared Allergens | 7 states |
| Food | CLASS III | Sliced Almonds recalled by El Ruisenor De Mexico | El Ruisenor De Mexico | Undeclared Allergens | 7 states |
| Food | CLASS III | Pecans in Shell recalled by El Ruisenor De MexicoPecans | El Ruisenor De Mexico | Undeclared Allergens | 7 states |
| Food | CLASS I | Primal Herbs, Volume, Herbal Supplement recalledPrimal Herbs | Primal Supplements Group | Hidden Drug Ingredients | NM |
| Food | CLASS II | Sempio Yellow Peach recalled by Sempio Food ServicesSempio Yellow | Sempio Food Services | Lead & Heavy Metals | 11 states |
| Food | CLASS II | Jovy Gummy Bears Neon recalled by El Ruisenor De MexicoJovy Gummy | El Ruisenor De Mexico | Undeclared Allergens | 7 states |
| Food | CLASS III | Wheat Germ recalled by El Ruisenor De Mexico | El Ruisenor De Mexico | Undeclared Allergens | 7 states |
| Food | CLASS III | Ground Shrimp recalled by El Ruisenor De Mexico | El Ruisenor De Mexico | Undeclared Allergens | 7 states |
| Food | CLASS III | Raw In-Shell Peanuts recalled by El Ruisenor De Mexico | El Ruisenor De Mexico | Undeclared Allergens | 7 states |
| Food | CLASS III | Natural Sesame Seeds recalled by El Ruisenor De Mexico | El Ruisenor De Mexico | Undeclared Allergens | 7 states |
| Food | CLASS II | Tropical Trail Mix recalled by El Ruisenor De MexicoTropical Trail | El Ruisenor De Mexico | Undeclared Sulfites | 7 states |
| Food | CLASS I | Broccoli Seeds Green Sprouting Calabrese recalled by Wild West SeedBroccoli | Wild West Seed | Salmonella | 11 states |
| Food | CLASS II | Marca El Pato Salsa para Enchiladas recalled by Walker FoodsMarca El | Walker Foods | Undeclared Allergens | Nationwide |
| Food | CLASS III | Roasted Whole Almonds recalled by El Ruisenor De Mexico | El Ruisenor De Mexico | Undeclared Allergens | 7 states |
| Food | CLASS III | Walnut halves recalled by El Ruisenor De Mexico | El Ruisenor De Mexico | Undeclared Allergens | 7 states |
| Food | CLASS III | Raw Shelled Pistachios recalled by El Ruisenor De Mexico | El Ruisenor De Mexico | Undeclared Allergens | 7 states |
| Food | CLASS II | Dried Pineapple Rings recalled by El Ruisenor De Mexico | El Ruisenor De Mexico | Undeclared Sulfites | 7 states |
| Food | CLASS III | Shelled White Pine Nuts recalled by El Ruisenor De MexicoShelled | El Ruisenor De Mexico | Undeclared Allergens | 7 states |
| Food | CLASS II | Dried Mango Slices recalled by El Ruisenor De Mexico | El Ruisenor De Mexico | Undeclared Sulfites | 7 states |
| Food | CLASS II | Jovy Gummy Peach Rings recalled by El Ruisenor De MexicoJovy Gummy | El Ruisenor De Mexico | Undeclared Allergens | 7 states |
| Food | CLASS II | Dried Peaches recalled by El Ruisenor De Mexico | El Ruisenor De Mexico | Undeclared Sulfites | 7 states |
| Food | CLASS III | Hulled Sesame Seeds recalled by El Ruisenor De MexicoHulled | El Ruisenor De Mexico | Undeclared Allergens | 7 states |
| Food | CLASS II | Air-Dried Apple Rings recalled by El Ruisenor De MexicoAir-Dried | El Ruisenor De Mexico | Undeclared Sulfites | 7 states |
| Food | CLASS II | Dried Fruit Mix recalled by El Ruisenor De Mexico | El Ruisenor De Mexico | Undeclared Sulfites | 7 states |
| Food | CLASS II | Amino Ultra, dietary supplement in white recalledAmino Ultra | Evexias Health Solution | Undeclared Fish & Shellfish | 9 states |
| Food | CLASS III | Dried Cod recalled by El Ruisenor De Mexico | El Ruisenor De Mexico | Undeclared Allergens | 7 states |
| Food | CLASS II | Gearharts Fine Chocolates products recalledGearharts Fine | Gearharts Fine Chocolates | Foreign Material | 17 states |
| Food | CLASS II | Dried Kiwi Slices recalled by El Ruisenor De Mexico | El Ruisenor De Mexico | Undeclared Sulfites | 7 states |
| Food | CLASS I | Bread Crumbs recalled by El Ruisenor De Mexico | El Ruisenor De Mexico | Undeclared Allergens | 7 states |
| Food | CLASS II | Whole Pitted Dried Apricots recalled by El Ruisenor De Mexico | El Ruisenor De Mexico | Undeclared Sulfites | 7 states |
| Food | CLASS III | Almond Flour recalled by El Ruisenor De Mexico | El Ruisenor De Mexico | Undeclared Allergens | 7 states |
| Food | CLASS III | Harina de Trigo recalled by El Ruisenor De MexicoHarina | El Ruisenor De Mexico | Undeclared Allergens | 7 states |
| Food | CLASS II | Crispy Rice Milk Chocolate Bar recalled by Trader Joe'sCrispy | Trader Joe's | Undeclared Wheat & Gluten | 12 states |
| Food | CLASS II | Fritura Lagrimita / Teardrop Wheat Snack recalledFritura Lagrimita | El Ruisenor De Mexico | Undeclared Allergens | 7 states |
| Food | CLASS II | Dried Diced Pineapple recalled by El Ruisenor De Mexico | El Ruisenor De Mexico | Undeclared Sulfites | 7 states |
| Food | CLASS II | Great Value Fruit Cocktail in Fruit Juice from Concentrate recalledGreat | Pacific Coast Producers | Lead & Heavy Metals | 7 states |
| Food | CLASS III | Butter Toffee Peanuts recalled by El Ruisenor De Mexico | El Ruisenor De Mexico | Undeclared Allergens | 7 states |
| Food | CLASS III | Wheat Bran recalled by El Ruisenor De Mexico | El Ruisenor De Mexico | Undeclared Allergens | 7 states |
| Food | CLASS II | Dried Pears recalled by El Ruisenor De Mexico | El Ruisenor De Mexico | Undeclared Sulfites | 7 states |
| Food | CLASS III | Wheat Snack recalled by El Ruisenor De Mexico | El Ruisenor De Mexico | Undeclared Allergens | 7 states |
| Food | CLASS III | Almonds in Shell recalled by El Ruisenor De MexicoAlmonds | El Ruisenor De Mexico | Undeclared Allergens | 7 states |
| Food | CLASS II | Jovy Gummy Bears Regular recalled by El Ruisenor De MexicoJovy Gummy | El Ruisenor De Mexico | Undeclared Allergens | 7 states |
| Food | CLASS II | Churro Mix recalled by El Ruisenor De MexicoChurro Mix | El Ruisenor De Mexico | Undeclared Allergens | 7 states |
| Food | CLASS I | Horchata Drink Mix recalled by El Ruisenor De MexicoHorchata | El Ruisenor De Mexico | Undeclared Allergens | 7 states |
| Food | CLASS III | Soybeans; packed in a clear plastic 1lb, 5lb, 50lb unit sizes. No recalledSoybeans | El Ruisenor De Mexico | Undeclared Allergens | 7 states |
| Food | CLASS I | Fritura Rueda Papa / Potato Wheel Snack recalledFritura Rueda | El Ruisenor De Mexico | Undeclared Allergens | 7 states |
| Food | CLASS II | All-Purpose Flour recalled by El Ruisenor De MexicoAll-Purpose | El Ruisenor De Mexico | Undeclared Allergens | 7 states |
| Food | CLASS II | Voila! juice 100% Squeezed Orange Voila! Oakland, CA recalledVoila | Voila Juice | Other | CA |
| Food | CLASS III | Textured Soy Protein recalled by El Ruisenor De MexicoTextured | El Ruisenor De Mexico | Undeclared Allergens | 7 states |
| Food | CLASS III | Wheat Snack recalled by El Ruisenor De Mexico | El Ruisenor De Mexico | Undeclared Allergens | 7 states |
| Food | CLASS III | Black Sesame Seeds recalled by El Ruisenor De Mexico | El Ruisenor De Mexico | Undeclared Allergens | 7 states |
| Food | CLASS II | Fritura mixed dry fruit recalled by El Ruisenor De MexicoFritura | El Ruisenor De Mexico | Undeclared Allergens | 7 states |
| Food | CLASS I | Special Red Almond Mole Powder recalled by El Ruisenor De MexicoSpecial | El Ruisenor De Mexico | Undeclared Allergens | 7 states |
| Food | CLASS III | Whole wheat flour recalled by El Ruisenor De Mexico | El Ruisenor De Mexico | Undeclared Allergens | 7 states |
| Food | CLASS II | Milk Chocolate Covered Raisins recalled by El Ruisenor De Mexico | El Ruisenor De Mexico | Undeclared Allergens | 7 states |
| Food | CLASS II | Jovy Gummy Worms Neon recalled by El Ruisenor De MexicoJovy Gummy | El Ruisenor De Mexico | Undeclared Allergens | 7 states |
| Device | CLASS II | Direxion Torqueable Microcatheter, Ngmc/Fathom/027/Straight/1RO/130 recalled | Boston Scientific Cork | Device Malfunction | Nationwide |
| Device | CLASS I | Vocsn+Pro recalled by Ventec Life Systems | Ventec Life Systems | Packaging Defects | Nationwide |
| Device | CLASS II | Medline Drape C-section W/Pouch ST 7/CS, Medline Product Number recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Techno-Path Multichem AE Unassayed Level recalled | Techno-path Manufacturing | Potency & Assay | Nationwide |
| Device | CLASS II | Direxion Torqueable Microcatheter, Ngmc/Single/021/Straight/1RO/130 recalled | Boston Scientific Cork | Device Malfunction | Nationwide |
| Device | CLASS I | VC+Pro recalled by Ventec Life Systems | Ventec Life Systems | Packaging Defects | Nationwide |
| Device | CLASS II | Direxion Torqueable Microcatheter, Ngmc/Single/021/Straight/2RO/155 recalled | Boston Scientific Cork | Device Malfunction | Nationwide |
| Device | CLASS II | Medline medical convenience kits labeled as recalled | Medline Industries | Other | Nationwide |
| Device | CLASS I | V*Home recalled by Ventec Life Systems | Ventec Life Systems | Packaging Defects | Nationwide |
| Device | CLASS I | V+Pro recalled by Ventec Life Systems | Ventec Life Systems | Packaging Defects | Nationwide |
| Device | CLASS II | Xact mole marker for mammography recalled by Solstice | Solstice | Other | Nationwide |
| Device | CLASS II | Direxion Torqueable Microcatheter, Ngmc/Single/021/Straight/2RO/130 recalled | Boston Scientific Cork | Device Malfunction | Nationwide |
| Device | CLASS II | Direxion Torqueable Microcatheter, Ngmc/Single/021/J/1RO/130 recalled | Boston Scientific Cork | Device Malfunction | Nationwide |
| Device | CLASS II | Medline medical convenience kits labeled as: Fetal Surgery Cds-lf recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Metatarsophalangeal (MTP) Implant is a sterile recalled by restor3d | restor3d | Sterility | Nationwide |
| Device | CLASS II | Medline Drape C-section Fen Clr Screen W, Medline Product Number recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Direxion Torqueable Microcatheter, Ngmc/Fathom/021/Bern/1RO/155 recalled | Boston Scientific Cork | Device Malfunction | Nationwide |
| Device | CLASS II | Direxion Torqueable Microcatheter, Ngmc/Transend/021/Bern/1RO/155 recalled | Boston Scientific Cork | Device Malfunction | Nationwide |
| Device | CLASS II | Direxion Torqueable Microcatheter, Ngmc/Single/027/J/1RO/155 recalled | Boston Scientific Cork | Device Malfunction | Nationwide |
| Device | CLASS II | Medline medical convenience kits labeled as: C-section Pack recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Direxion Torqueable Microcatheter, Ngmc/Fathom/021/Bern/1RO/130 recalled | Boston Scientific Cork | Device Malfunction | Nationwide |
| Device | CLASS II | Medline medical convenience kits labeled as recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Direxion Torqueable Microcatheter, Ngmc/Single/027/Bern/1RO/105 recalled | Boston Scientific Cork | Device Malfunction | Nationwide |
| Device | CLASS II | Halyard Anterior Hip Pack recalled by Avid Medical | Avid Medical | Sterility | Nationwide |
| Device | CLASS II | Rotor Assy-SW41, Reference Number recalled by Beckman Coulter | Beckman Coulter | Device Malfunction | Nationwide |
| Device | CLASS II | Amplatzer Amulet Left Atrial Appendage Occluder recalled by Abbott | Abbott | Other | Nationwide |
| Device | CLASS II | Medline Drape C-sec Fen Clear Scrn Wire, Medline Product Number recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Direxion Torqueable Microcatheter, Ngmc/Single/027/Swan/1RO/155 recalled | Boston Scientific Cork | Device Malfunction | Nationwide |
| Device | CLASS II | Direxion Torqueable Microcatheter, Ngmc/Single/027/J/1RO/130 recalled | Boston Scientific Cork | Device Malfunction | Nationwide |
| Device | CLASS II | Techno-Path Multichem AE Unassayed Level recalled | Techno-path Manufacturing | Potency & Assay | Nationwide |
| Device | CLASS I | VC Model Number: Prt-01098-000, Package PN:Prt-01125-000. used recalled | Ventec Life Systems | Packaging Defects | Nationwide |
| Device | CLASS II | Direxion Torqueable Microcatheter, Ngmc/Fathom/021/Straight/2RO/130 recalled | Boston Scientific Cork | Device Malfunction | Nationwide |
| Device | CLASS II | Direxion Torqueable Microcatheter, Ngmc/Fathom/021/Bern/2RO/130 recalled | Boston Scientific Cork | Device Malfunction | Nationwide |
| Device | CLASS I | Philips Lumify Diagnostic Ultrasound System recalled | Philips Ultrasound | Other | Nationwide |
| Device | CLASS II | Direxion Torqueable Microcatheter, Ngmc/Fathom/021/Straight/1RO/130 recalled | Boston Scientific Cork | Device Malfunction | Nationwide |
| Device | CLASS II | Direxion Torqueable Microcatheter, Ngmc/Fathom/021/Straight/1RO/155 recalled | Boston Scientific Cork | Device Malfunction | Nationwide |
| Device | CLASS I | VC+Pro (Japan) recalled by Ventec Life Systems | Ventec Life Systems | Packaging Defects | Nationwide |
| Device | CLASS II | Medtronic NDI Passive Spheres recalled by Medtronic Navigation | Medtronic Navigation | Sterility | 44 states |
| Device | CLASS II | Direxion Torqueable Microcatheter, Ngmc/Single/027/Straight/1RO/105 recalled | Boston Scientific Cork | Device Malfunction | Nationwide |
| Device | CLASS I | Vocsn+Pro (Japan) recalled by Ventec Life Systems | Ventec Life Systems | Packaging Defects | Nationwide |
| Device | CLASS II | Medline medical convenience kits labeled as recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Direxion Torqueable Microcatheter, Ngmc/Fathom/027/Straight/1RO/155 recalled | Boston Scientific Cork | Device Malfunction | Nationwide |
| Device | CLASS II | Halyard Anterior Hip Pack recalled by Avid Medical | Avid Medical | Sterility | Nationwide |
| Device | CLASS I | Vocsn Model Number: Prt recalled by Ventec Life Systems | Ventec Life Systems | Packaging Defects | Nationwide |
| Device | CLASS II | Philips Smart-hopping 2.0 AP 1.4 GHz recalled by Philips North America | Philips North America | Other | Nationwide |
| Device | CLASS II | Medline medical convenience kits labeled as recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Direxion Torqueable Microcatheter, Ngmc/Fathom/027/Bern/1RO/130 recalled | Boston Scientific Cork | Device Malfunction | Nationwide |
| Device | CLASS II | PNE Lead Implant Kit recalled by Axonics | Axonics | Packaging Defects | Nationwide |
| Device | CLASS II | Direxion Torqueable Microcatheter, Ngmc/Single/021/Bern/1RO/155 recalled | Boston Scientific Cork | Device Malfunction | Nationwide |
| Device | CLASS II | B Braun Safsite Injection Site, RV1000NC Safsite Valve W/O Extra Cap recalled | B Braun Medical | Packaging Defects | Nationwide |
| Device | CLASS II | Direxion Torqueable Microcatheter, Ngmc/Single/021/Swan/1RO/155 recalled | Boston Scientific Cork | Device Malfunction | Nationwide |
| Device | CLASS II | Direxion Torqueable Microcatheter, Ngmc/Single/027/Swan/1RO/130 recalled | Boston Scientific Cork | Device Malfunction | Nationwide |
| Device | CLASS II | Square Driver recalled by Think Surgical | Think Surgical | Other | Nationwide |
| Device | CLASS II | Direxion Torqueable Microcatheter, Ngmc/Single/027/Straight/1RO/130 recalled | Boston Scientific Cork | Device Malfunction | Nationwide |
| Device | CLASS II | Medline medical convenience kits labeled as recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Direxion Torqueable Microcatheter, Ngmc/Single/021/Straight/1RO/155 recalled | Boston Scientific Cork | Device Malfunction | Nationwide |
| Device | CLASS I | VCSN+Pro recalled by Ventec Life Systems | Ventec Life Systems | Packaging Defects | Nationwide |
| Device | CLASS II | CareLink Clinic recalled by Medtronic MiniMed | Medtronic MiniMed | Device Malfunction | Nationwide |
| Device | CLASS II | Direxion Torqueable Microcatheter, Ngmc/Single/021/Straight/1RO/105 recalled | Boston Scientific Cork | Device Malfunction | Nationwide |
| Device | CLASS II | Direxion Torqueable Microcatheter, Ngmc/Single/027/Straight/1RO/155 recalled | Boston Scientific Cork | Device Malfunction | Nationwide |
| Device | CLASS II | Direxion Torqueable Microcatheter, Ngmc/Single/021/Bern/2RO/155 recalled | Boston Scientific Cork | Device Malfunction | Nationwide |
| Device | CLASS II | Direxion Torqueable Microcatheter, Ngmc/Transend/027/Bern/1RO/130 recalled | Boston Scientific Cork | Device Malfunction | Nationwide |
| Device | CLASS II | Direxion Torqueable Microcatheter recalled by Boston Scientific Cork | Boston Scientific Cork | Device Malfunction | Nationwide |
| Device | CLASS II | Direxion Torqueable Microcatheter, Ngmc/Single/027/Bern/1RO/155 recalled | Boston Scientific Cork | Device Malfunction | Nationwide |
| Device | CLASS II | Direxion Torqueable Microcatheter, Ngmc/Single/021/Bern/1RO/105 recalled | Boston Scientific Cork | Device Malfunction | Nationwide |
| Device | CLASS II | Direxion Torqueable Microcatheter, Ngmc/Single/021/Swan/1RO/130 recalled | Boston Scientific Cork | Device Malfunction | Nationwide |
| Device | CLASS II | Direxion Torqueable Microcatheter recalled by Boston Scientific Cork | Boston Scientific Cork | Device Malfunction | Nationwide |
| Device | CLASS II | Direxion Torqueable Microcatheter, Ngmc/Single/021/Bern/2RO/130 recalled | Boston Scientific Cork | Device Malfunction | Nationwide |
| Device | CLASS II | Direxion Torqueable Microcatheter, Ngmc/Single/021/Bern/1RO/130 recalled | Boston Scientific Cork | Device Malfunction | Nationwide |
| Device | CLASS II | Medtronic NDI Passive Spheres recalled by Medtronic Navigation | Medtronic Navigation | Sterility | 44 states |
| Device | CLASS II | InterStim Percutaneous Extensions Ext 3560022 Istm II Perc recalled | Medtronic Neuromodulation | Other | Nationwide |
| Device | CLASS II | Direxion Torqueable Microcatheter, Ngmc/Transend/021/Bern/1RO/130 recalled | Boston Scientific Cork | Device Malfunction | Nationwide |
| Device | CLASS II | Rotor Assy-SW40, Reference Number recalled by Beckman Coulter | Beckman Coulter | Device Malfunction | Nationwide |
| Device | CLASS II | Techno-Path Multichem AE Unassayed Level recalled | Techno-path Manufacturing | Potency & Assay | Nationwide |
| Device | CLASS II | The MiniMed Go app for iOS or MiniMed Go app recalled | Medtronic MiniMed | Device Malfunction | Nationwide |
| Device | CLASS II | Vacuette LH Lithium Heparin Separator recalled | Greiner Bio-One North America | Other | Nationwide |
| Device | CLASS I | VC(Japan) recalled by Ventec Life Systems | Ventec Life Systems | Packaging Defects | Nationwide |
| Device | CLASS II | Medline medical convenience kits labeled as (list truncated) recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Medtronic NDI Passive Spheres recalled by Medtronic Navigation | Medtronic Navigation | Sterility | 44 states |
| Device | CLASS II | Direxion Torqueable Microcatheter, Ngmc/Single/021/J/1RO/105 recalled | Boston Scientific Cork | Device Malfunction | Nationwide |
| Device | CLASS I | V+ Pro Emergency recalled by Ventec Life Systems | Ventec Life Systems | Packaging Defects | Nationwide |
| Device | CLASS II | Medline medical convenience kits labeled as: Hip Scope Pack recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Medtronic Biopsy Needle Kit recalled by Medtronic Navigation | Medtronic Navigation | Sterility | 44 states |
| Device | CLASS I | Vocsn (Japan) recalled by Ventec Life Systems | Ventec Life Systems | Packaging Defects | Nationwide |
| Device | CLASS II | Direxion Torqueable Microcatheter, Ngmc/Single/021/J/1RO/155 recalled | Boston Scientific Cork | Device Malfunction | Nationwide |
| Device | CLASS II | Ion Torrent Genexus Dx recalled by Life Technologies Holdings Pte | Life Technologies Holdings Pte | Device Malfunction | Nationwide |
| Device | CLASS II | Direxion Torqueable Microcatheter, Ngmc/Fathom/027/Bern/1RO/155 recalled | Boston Scientific Cork | Device Malfunction | Nationwide |
| Device | CLASS II | Direxion Torqueable Microcatheter, Ngmc/Single/027/Bern/1RO/130 recalled | Boston Scientific Cork | Device Malfunction | Nationwide |
| Device | CLASS II | Direxion Torqueable Microcatheter, Ngmc/Single/021/Swan/1RO/105 recalled | Boston Scientific Cork | Device Malfunction | Nationwide |
| Drug | CLASS II | Brush Buddies, Cookies 'n Cream Ice Cream Flavored recalled | Pritam International Private | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Brush Buddies, Whitening Anti-cavity Fluoride Toothpaste recalled | Pritam International Private | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Brush Buddies, Crayola, Silly Scents recalled | Pritam International Private | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Levoxyl (levothyroxine sodium tablets, USP), tablets, 175 mcg recalledLevoxyl | Pfizer | Potency & Assay | Nationwide |
| Drug | CLASS II | Testosterone Cypionate, 200 mg/mL recalled by Right Value Drug Stores | Right Value Drug Stores | Sterility | Nationwide |
| Drug | CLASS II | Brush Buddies, Barbie, Anticavity Fluoride Toothpaste recalled | Pritam International Private | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Brush Buddies, Vanilla Ice Cream Flavored Toothpaste recalled | Pritam International Private | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | ARU, Toothpaste, Cavity Protection, 9 Ingredients recalled | Pritam International Private | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Amlodipine and Olmesartan Medoxomil Tablets, 10mg/40mg recalledAmlodipine And Olmesartan Medoxomil | Ascend Laboratories | Potency & Assay | Nationwide |
| Drug | CLASS II | evo, Advanced Whitening, Anticavity Fluoride Toothpaste recalled | Pritam International Private | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Levoxyl (levothyroxine sodium tablets, USP), tablets, 175 mcg recalledLevoxyl | Pfizer | Potency & Assay | Nationwide |
| Drug | CLASS II | Brush Buddies, Chocolate Ice Cream Flavored Toothpaste recalled | Pritam International Private | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS I | Argatroban Injection, USP, 250 mg/ (100 mg/mL) x Dose Vial recalledArgatroban | Par Health USA | Particulate Matter | Nationwide |
| Drug | CLASS III | Telmisartan and Amlodipine, Tablets, USP, 40mg/5 mg recalled by ViatrisTelmisartan And Amlodipine | Viatris | Potency & Assay | Nationwide |
| Drug | CLASS II | ARU, Toothpaste, Gum Health, 9 Ingredients, Soothing Mint recalled | Pritam International Private | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Brush Buddies, Crayola Silly Scents recalled | Pritam International Private | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Heparin Sodium Injection recalled by Shenzhen TechdowHeparin Sodium | Shenzhen Techdow Pharmaceutical | Sterility | Nationwide |
| Drug | CLASS II | Abirtega (abiraterone acetate) USP, 250 mg recalledAbirtega | Hikma Pharmaceuticals USA | Other | Nationwide |
| Drug | CLASS II | Brush Buddies, Hot Wheels, Anticavity Fluoride Toothpaste recalled | Pritam International Private | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Cinacalcet Tablets, 30 mg recalled by Strides PharmaCinacalcet | Strides Pharma | Potency & Assay | Nationwide |
| Drug | CLASS II | BB (Brush Buddies) Cavity Protection recalled | Pritam International Private | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Brush Buddies, My Little Pony Scents Anticavity Fluoride recalled | Pritam International Private | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | BB (Brush Buddies) Advanced Whitening recalled | Pritam International Private | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Brush Buddies, Crayola, Silly Scents recalled | Pritam International Private | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | evo, Sensitive, Anticavity Fluoride Toothpaste recalled | Pritam International Private | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Brush Buddies, Mint Chocolate Chip Ice Cream Flavored recalled | Pritam International Private | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS I | Argatroban Injection, USP, 250 mg/ (100 mg/mL) x Dose Vial recalledArgatroban | Par Health USA | Particulate Matter | Nationwide |
| Food | CLASS I | Gardners Basics Waltham 29 Broccoli Sprouting Seeds recalledGardners Basics | Gardeners Basics | Salmonella | Nationwide |
| Food | CLASS II | Babies' Magic Tea recalled by Pacific Health SciencesBabies' Magic | Pacific Health Sciences | Other | FL |
| Food | CLASS I | Heirloom Homegrown Green Sprouting Calabrese Broccoli Sprouts Seed recalledHeirloom Homegrown | EAK Distribution | Salmonella | Nationwide |
| Drug | CLASS I | Glutathione Injection (Glutathione-L, Ascorbic Acid recalled | Greenwich Rx | Sterility | Nationwide |
| Food | ANNOUNCED | H-e-b BBQ Chop Salad Kit recalled by Taylor FarmsH-E-B | Taylor Farms | Undeclared Tree Nuts | TX |
| Food | ANNOUNCED | No Brand Cold Smoked Sprat Fish recalled by D&M Smoked FishNo Brand | D&M Smoked Fish | Botulism | NJ, NY, PA |
| Food | CLASS I | Beef Jerky Products recalled by Imperio Distribution | Imperio Distribution | Undeclared Allergens | |
| Food | ANNOUNCED | Ultimate Forza Male Supplement recalled by Tonight We RideUltimate Forza | Tonight We Ride | Undeclared Allergens | |
| Food | ANNOUNCED | Natural Grocers Mung Beans recalled by Vitamin Cottage Natural FoodNatural Grocers | Vitamin Cottage Natural Food Markets | Foreign Material | 22 states |
| Food | ANNOUNCED | Hoagie Rolls recalled by WinCo FoodsWinCo Foods | WinCo Foods | Undeclared Sesame | 7 states |
| Food | CLASS I | Pear and Pecorino Triangoli Ravioli recalled by Deano's PastaPear | Deano's Pasta | Undeclared Allergens | MA, NH |
| Food | CLASS II | Holsum Spinach Flour Tortillas Large recalled by Holsum De Puerto RicoHolsum | Holsum De Puerto Rico | Undeclared Allergens | PR |
| Food | CLASS II | Stewarts Shops Vanilla chocolate Strawberry Ice Cream recalledStewarts Shops | Stewart's Shops | Foreign Material | NH, NY, VT |
| Food | CLASS II | Made From Plants recalled by Daring FoodsMade From | Daring Foods | Packaging Defects | FL, NC |
| Food | CLASS III | Pur Aqua Sparkling Frost Cherry Limeade recalledPur Aqua | Refresco Beverages US | Undeclared Allergens | FL |
| Food | CLASS II | Stewarts Shops Vanilla Heavenly Medley recalledStewarts Shops | Stewart's Shops | Foreign Material | NH, NY, VT |
| Device | CLASS II | Rapicide PA Part A High-Level Disinfectant recalled by Steris | Steris | Other | Nationwide |
| Device | CLASS II | NeuroStar Advanced Therapy System recalled by Neuronetics | Neuronetics | Other | Nationwide |
| Device | CLASS II | Medline surgical convenience kits labeled as: EAR recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | NaviFlex LW Pusher recalled by Boston Scientific | Boston Scientific | Other | Nationwide |
| Device | CLASS II | Multiple-type respiratory pathogen nucleic acid IVD, kit recalled | BioFire Diagnostics | Device Malfunction | Nationwide |
| Device | CLASS II | TS Misc. Instruments Tray, Triathlon recalled by Howmedica Osteonics | Howmedica Osteonics | Sterility | NJ |
| Device | CLASS II | BD Phoenix Panel Nmic recalled by Becton Dickinson | Becton Dickinson | Device Malfunction | Nationwide |
| Device | CLASS II | JenaValve Trilogy Delivery Catheter, Size recalled | Jenavalve Technology | Other | Nationwide |
| Device | CLASS II | Convenience Kits containing Conmed AirSeal Access Ports recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | Medline surgical convenience kits labeled as recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | Scout MD recalled by Merit Medical Systems | Merit Medical Systems | Other | 7 states |
| Device | CLASS II | BD Phoenix Panel Nmic recalled by Becton Dickinson | Becton Dickinson | Device Malfunction | Nationwide |
| Device | CLASS II | Convenience Kits containing Conmed AirSeal Access Ports recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | Curaplex Capnography EtCO2/O2 Oral/Nasal Cannula Multipack recalled | Sarnova HC | Other | Nationwide |
| Device | CLASS II | Convenience Kits containing Conmed AirSeal Access Ports recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | Product Name Aud Open Heart Pack, Medline Kit Number recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | Multiple-type respiratory pathogen nucleic acid IVD, kit recalled | BioFire Diagnostics | Device Malfunction | Nationwide |
| Device | CLASS II | Forward Gunshot Wound Kit recalled by Integrated Medcraft | Integrated Medcraft | Sterility | Nationwide |
| Device | CLASS II | Rapicide PA Part A High-Level Disinfectant recalled by Steris | Steris | Other | Nationwide |
| Device | CLASS II | Medline surgical convenience kits labeled as recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | Perma-hand Silk Black Braided Sterile Nonabsorbable recalled by Ethicon | Ethicon | Packaging Defects | Nationwide |
| Device | CLASS II | JenaValve Trilogy Delivery Catheter, Size recalled | Jenavalve Technology | Other | Nationwide |
| Device | CLASS II | The Gore Viabil Short Wire Biliary Endoprosthesis recalled | W L Gore & Associates | Labeling Errors | Nationwide |
| Device | CLASS II | MAS Omni Immune PRO Liquid Assayed Integrated Immunoassay recalled | Microgenics | Potency & Assay | Nationwide |
| Device | CLASS II | Rapicide PA Part A High-Level Disinfectant recalled by Steris | Steris | Other | Nationwide |
| Device | CLASS II | JenaValve Trilogy Delivery Catheter, Size recalled | Jenavalve Technology | Other | Nationwide |
| Device | CLASS II | IQ200 Sprint recalled by Beckman Coulter | Beckman Coulter | Packaging Defects | Nationwide |
| Device | CLASS II | Medline surgical convenience kits labeled as: Spinal CDS recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | REF: P65 ST862 CoLag Screw, FT, 6.7X62.5 mm recalled by In2bones USA | In2bones USA | Labeling Errors | Nationwide |
| Device | CLASS II | iFuse TORQ Implant System recalled by Si-bone | Si-bone | Sterility | Nationwide |
| Device | CLASS II | Iomax Cortical Module recalled by Cadwell Industries | Cadwell Industries | Device Malfunction | Nationwide |
| Device | CLASS II | The ABL90 Flex and ABL90 Flex Plus analyzers are intended recalled | Radiometer Medical ApS | Labeling Errors | Nationwide |
| Device | CLASS II | Convenience Kits containing Conmed AirSeal Access Ports Kit recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | Medline surgical convenience kits labeled as recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | TS Femoral Prep Tray, Triathlon recalled by Howmedica Osteonics | Howmedica Osteonics | Sterility | NJ |
| Device | CLASS II | IntelePACS, InteleConnect Portal/Tech Portal Versions recalled | Intelerad Medical Systems | Device Malfunction | Nationwide |
| Device | CLASS I | HemoslL AcuStar HIT-lgG(PF-4) recalled by Instrumentation Laboratory | Instrumentation Laboratory | Other | Nationwide |
| Device | CLASS II | Mulitple-type osteoarticular pathogen nucleic acid IVD, kit recalled | BioFire Diagnostics | Device Malfunction | Nationwide |
| Device | CLASS II | Grafton" DBM and Grafton Plus" DBM contain demineralized recalled | Medtronic Sofamor Danek USA | Other Bacterial Contamination | Nationwide |
| Device | CLASS II | Medline surgical convenience kits labeled as recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | Medline surgical convenience kits labeled as recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | Convenience Kits containing Conmed AirSeal Access Ports Chn recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | DxU 840m Iris recalled by Beckman Coulter | Beckman Coulter | Packaging Defects | Nationwide |
| Device | CLASS II | Likorall Overhead Lifts Product Code: 3121001 Product Description recalled | Baxter Healthcare | Device Malfunction | Nationwide |
| Device | CLASS III | LeadCare II Blood Lead Test Kit recalled by Magellan Diagnostics | Magellan Diagnostics | Other | Nationwide |
| Device | CLASS II | Medline surgical convenience kits labeled as recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | Medline surgical convenience kits labeled as: Open Heart recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | Convenience Kits containing Conmed AirSeal Access Ports recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | Medline convenience kit labeled as: Foot Ankle recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Grafton" DBM and Grafton Plus" DBM contain demineralized recalled | Medtronic Sofamor Danek USA | Other Bacterial Contamination | Nationwide |
| Device | CLASS II | Williams Cystoscopic Injection Needles, used recalled by Cook | Cook | Device Malfunction | 5 states |
| Device | CLASS I | HemoslL AcuStar HIT-lgG(PF-4) recalled by Instrumentation Laboratory | Instrumentation Laboratory | Other | Nationwide |
| Device | CLASS II | Triathlon Hinge Femoral Prep Tray recalled by Howmedica Osteonics | Howmedica Osteonics | Sterility | NJ |
| Device | CLASS II | Power F2 Powered Fastening System, Power F2 recalled by Ferno-Washington | Ferno-Washington | Potency & Assay | Nationwide |
| Device | CLASS II | TS Universal Baseplate Finishing Tray, Triathlon recalled | Howmedica Osteonics | Sterility | NJ |
| Drug | CLASS II | Tirzepatide/Niacinamide vial (40 MG per Vial) Inj 20mg/2mg/mL recalled | Houston Rx | Sterility | Nationwide |
| Drug | CLASS II | Hydrocortisone Sodium Succinate for Injection recalledHydrocortisone Sodium Succinate | Zydus Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS II | Metoclopramide Tablets, USP, 5 mg (10 recalledMetoclopramide | American Health Packaging | Packaging Defects | Nationwide |
| Drug | CLASS II | Metoclopramide Tablets, USP, 5 mg, [100 or 500] Tablets recalledMetoclopramide | Teva Pharmaceuticals USA | Other | Nationwide |
| Drug | CLASS II | Sermorelin, 1 mg/mL vial, Sterile injectable solution recalled | Houston Rx | Other | Nationwide |
| Drug | ANNOUNCED | No Brand Name Compounded veterinary medications recalledNo Brand Name | Wedgewood Pharmacy | Potency & Assay | Nationwide |
| Food | CLASS II | J. Higgs Loaded Bacon & Cheddar Potato Chips recalledJ. Higgs | Saratoga Potato Chips | Undeclared Soy | 6 states |
| Food | CLASS I | Meat and Poultry Products recalled by Kayem Foods | Kayem Foods | Temperature Abuse | |
| Food | ANNOUNCED | Gelatelli Coffee & Vanilla Gelato with Coffee Sauce & Cookie Pieces recalledGelatelli | Lidl US | Listeria | 10 states |
| Food | ANNOUNCED | Family Farmstead Raw Mild Cheddar Cheese recalledFamily Farmstead | Family Farmstead Dairy | E. coli | |
| Food | ANNOUNCED | Family Farmstead Raw Mild Cheddar Cheese recalledFamily Farmstead | Family Farmstead Dairy | E. coli | NJ, NY |
| Food | CLASS II | Elevated Edibles Hybrid Gum Drops - Passion Guava Kush 140mg THC recalledElevated Edibles | Sweet Sensi | Other Bacterial Contamination | Nationwide |
| Food | CLASS II | Gatorade Lemon Lime Zero, and Gatorade Orange Zero recalled by PepsicoGatorade | Pepsico | Undeclared Allergens | 37 states |
| Food | CLASS II | Frozen Mushroom & Onion Pizza recalled by Saint Francis Apizza | Saint Francis Apizza | Undeclared Soy | KY, OH |
| Food | CLASS I | Leasa Living Alfalfa Sprouts recalled by Leasa IndustriesLeasa Living | Leasa Industries | E. coli | FL, NH |
| Food | CLASS II | Lemon Blueberry Loaf recalled by J K Patisserie & Bakery | J K Patisserie & Bakery | Undeclared Soy | NJ, NY |
| Food | CLASS I | biQ-FEL recalled by A&P Creations | A&P Creations | Undeclared Allergens | Nationwide |
| Food | CLASS II | Frozen Supreme Pizza recalled by Saint Francis Apizza | Saint Francis Apizza | Undeclared Soy | KY, OH |
| Food | CLASS I | Donutful Chocolate Dipped Vanilla Cake Donuts -/Case recalledDonutful | The Better Bakehouse Snack | Undeclared Milk | Nationwide |
| Food | CLASS I | Lemon Alfredo Fettuccine recalled by Gias Food | Gias Food | Listeria | Nationwide |
| Food | CLASS II | Frozen Cheese Pizza recalled by Saint Francis Apizza | Saint Francis Apizza | Undeclared Soy | KY, OH |
| Food | CLASS II | Croissant; packaged in cardboard box; Ingredients recalledCroissant | J K Patisserie & Bakery | Undeclared Egg | NJ, NY |
| Food | CLASS I | Leasa Alfalfa Sprouts recalled by Leasa IndustriesLeasa Alfalfa | Leasa Industries | E. coli | FL, NH |
| Food | CLASS II | Chocolate Chip Cookies recalled by J K Patisserie & Bakery | J K Patisserie & Bakery | Undeclared Soy | NJ, NY |
| Food | CLASS II | Pastel de Queso (Cheese Pie) recalled by Queso Palmita GPPastel | Queso Palmita GP | Undeclared Milk | TX |
| Device | CLASS II | Plastics Tray kits recalled by Avid Medical | Avid Medical | Foreign Material | Nationwide |
| Device | CLASS III | Passport Series Patient Monitor recalled by Mindray DS USA | Mindray DS USA | Device Malfunction | Nationwide |
| Device | CLASS II | Heart Prep Tray kits recalled by Avid Medical | Avid Medical | Other | Nationwide |
| Device | CLASS II | Pack Open Heart Cfh kits recalled by Avid Medical | Avid Medical | Other | Nationwide |
| Device | CLASS II | TufTex¿ Over-the-Wire Embolectomy Catheter recalled | LeMaitre Vascular | Other | Nationwide |
| Device | CLASS III | T1 Patient Monitor recalled by Mindray DS USA | Mindray DS USA | Device Malfunction | Nationwide |
| Device | CLASS II | Sperm Ab Elisa (96 well plate test) recalled by DRG International | DRG International | Other | Nationwide |
| Device | CLASS II | Intellijoint Navigation System: Workstation G2 Configured recalled | Intellijoint Surgical | Device Malfunction | Nationwide |
| Device | CLASS II | Adaptable Beach Chair Beach Chair surgical patient positioner recalled | Quantum OPS | Device Malfunction | Nationwide |
| Device | CLASS II | Laparoscopic Prostatectomy kits recalled by Avid Medical | Avid Medical | Other | Nationwide |
| Device | CLASS III | BeneView Series recalled by Mindray DS USA | Mindray DS USA | Device Malfunction | Nationwide |
| Device | CLASS III | cPM Series Patient Monitor recalled by Mindray DS USA | Mindray DS USA | Device Malfunction | Nationwide |
| Device | CLASS II | DxC 500 AU Clinical Chemistry Analyzers: AU w/out ISE recalled | Beckman Coulter | Device Malfunction | Nationwide |
| Device | CLASS II | Alphenix Infx-8000C/B5 recalled by Canon Medical System USA | Canon Medical System USA | Other | Nationwide |
| Device | CLASS II | Halyard Laparoscopy Comprehensive Pack II recalled | GRI Medical & Electronic Technology | Other | Nationwide |
| Device | CLASS II | Endovascular Pack kits recalled by Avid Medical | Avid Medical | Other | Nationwide |
| Device | CLASS III | BeneVision Series Telemetry Monitor recalled by Mindray DS USA | Mindray DS USA | Device Malfunction | Nationwide |
| Device | CLASS II | Davinci LAP/GYN kits recalled by Avid Medical | Avid Medical | Other | Nationwide |
| Device | CLASS II | Sediplast; Model/Catalog Numbers recalled by Polymedco, Inc. / Polymedco | Polymedco, Inc. / Polymedco Cancer Diagnostic Products | Other | Nationwide |
| Device | CLASS II | DxC 500i Clinical Analyzer Modules: DxC 500 AU Module w/ISE recalled | Beckman Coulter | Device Malfunction | Nationwide |
| Device | CLASS II | Presource Packs containing Medtronic Microstream Components recalled | Cardinal Health 200 | Device Malfunction | IL |
| Device | CLASS III | Panorama and Telemetry Monitoring System recalled by Mindray DS USA | Mindray DS USA | Device Malfunction | Nationwide |
| Device | CLASS II | Major Pack kits recalled by Avid Medical | Avid Medical | Other | Nationwide |
| Device | CLASS III | Kit: Urinary Clean Catch 20/cs recalled by Medical Action Industries | Medical Action Industries Inc. 306 | Device Malfunction | CA |
| Device | CLASS II | Gyn Laparoscopy/Laparotomy kits recalled by Avid Medical | Avid Medical | Other | Nationwide |
| Device | CLASS III | BeneVision N1 and N-Series Patient Monitor recalled by Mindray DS USA | Mindray DS USA | Device Malfunction | Nationwide |
| Device | CLASS II | ABD Hysterectomy kits recalled by Avid Medical | Avid Medical | Other | Nationwide |
| Device | CLASS II | Gyn Laparoscopy Pack kits recalled by Avid Medical | Avid Medical | Other | Nationwide |
| Device | CLASS II | Rollator, Bariatric, Basic Steel, Burgundy recalled | Medline Industries | Foreign Material | Nationwide |
| Device | CLASS II | Verify Biological Steam Test Pack recalled by Steris | Steris | Sterility | Nationwide |
| Device | CLASS II | Davinci Trucustom Bundle kits recalled by Avid Medical | Avid Medical | Other | Nationwide |
| Device | CLASS III | ePM Series Patient Monitor recalled by Mindray DS USA | Mindray DS USA | Device Malfunction | Nationwide |
| Device | CLASS II | Urology Major kits recalled by Avid Medical | Avid Medical | Other | Nationwide |
| Device | CLASS II | HexaVue Focus Integration System, a single recalled by Steris | Steris | Device Malfunction | Nationwide |
| Device | CLASS II | Craniotomy Pack kits recalled by Avid Medical | Avid Medical | Other | Nationwide |
| Device | CLASS II | My3D Personalized Pelvic Implant, Porous, Left recalled | Onkos Surgical | Other | Nationwide |
| Device | CLASS II | Adult Heart Tray Shands Jacks kits recalled by Avid Medical | Avid Medical | Other | Nationwide |
| Device | CLASS II | Verify Biological/Integrator Challenge Pack recalled by Steris | Steris | Sterility | Nationwide |
| Device | CLASS II | Robotic Prostatectomy Pack kits recalled by Avid Medical | Avid Medical | Other | Nationwide |
| Device | CLASS II | Verify Dual Species Self-Contained Biological Indicator recalled | Steris | Sterility | Nationwide |
| Device | CLASS II | Glypto Device, Glypto Cryo Machine recalled by Limitless Cryo | Limitless Cryo | Other | Nationwide |
| Device | CLASS II | Verify Dual Species Self-Contained Biological Indicator recalled | Steris | Sterility | Nationwide |
| Device | CLASS II | Verify Biological/Integrator Challenge Pack recalled by Steris | Steris | Sterility | Nationwide |
| Device | CLASS II | Battle Bandage recalled by Safeguard US Operating | Safeguard US Operating | Foreign Material | Nationwide |
| Device | CLASS II | Nihon Kohden CNS-6200 Series Central Nurse Station recalled | Nihon Kohden America | Device Malfunction | Nationwide |
| Device | CLASS II | My3D Personalized Pelvic Implant, Porous, Left recalled | Onkos Surgical | Other | Nationwide |
| Device | CLASS II | Rollator, Bariatric, Basic Steel, Blue recalled by Medline Industries | Medline Industries | Foreign Material | Nationwide |
| Device | CLASS II | Spectral CT and Spectral CT 7500 RT recalled by Philips Medical Systems | Philips Medical Systems | Device Malfunction | Nationwide |
| Device | CLASS II | MiniMed Flex Insulin Pump recalled by Medtronic MiniMed | Medtronic MiniMed | Labeling Errors | Nationwide |
| Device | CLASS II | Verify Biological Steam Test Pack recalled by Steris | Steris | Sterility | Nationwide |
| Device | CLASS II | Bard Ep Xt Decapolar Steerable, Diagnostic Ep Catheter, 6f recalled | Stryker Sustainability Solutions | Particulate Matter | Nationwide |
| Drug | CLASS II | Apothecary NAD+ Injection 200 mg/mL Sterile Multi-Dose Vial recalled | Apothecary Pharma | Sterility | Nationwide |
| Drug | CLASS II | Sterile Eye Drops Redness Relief (Glycerin recalledLeader Eye Drops Redness Relief | K.C. Pharmaceuticals | Sterility | Nationwide |
| Drug | CLASS II | Sermorelin Acetate 1 MG/ML Injectable recalled by Carolina Infusion | Carolina Infusion | Sterility | Nationwide |
| Drug | CLASS II | Semaglutide 3 MG/ML Injectable, . syringes recalled by Carolina Infusion | Carolina Infusion | Sterility | Nationwide |
| Drug | CLASS II | Semaglutide/cyanocobalamin 3/2 MG/ML Injectable recalled | Carolina Infusion | Sterility | Nationwide |
| Drug | CLASS II | Sterile EYE Drops AC (tetrahydrozoline HCl recalledGoodsense Eye Drops Irritation Relief | K.C. Pharmaceuticals | Sterility | Nationwide |
| Drug | CLASS III | Tretinoin Cream USP, 0.05% tube recalledTretinoin | SUN Pharmaceutical Industries | Potency & Assay | Nationwide |
| Drug | CLASS II | Semaglutide/cyanocobalamin 9/2 MG/ML Injectable recalled | Carolina Infusion | Sterility | Nationwide |
| Drug | CLASS II | Artificial Tears Sterile Lubricant Eye Drops recalledLeader Artificial Tears 15 Ml | K.C. Pharmaceuticals | Sterility | Nationwide |
| Drug | CLASS II | Tirzepatide 26 MG/ML Injectable recalled by Carolina Infusion | Carolina Infusion | Sterility | Nationwide |
| Drug | CLASS II | Tris/Tromethamine, USP, GMP, API Grade recalled by BioSpectra | BioSpectra | Potency & Assay | CA |
| Drug | CLASS II | Tirzepatide/cyanocobalamin 76/2 MG/ML Injectable recalled | Carolina Infusion | Sterility | Nationwide |
| Drug | CLASS II | Eye Drops Maximum, Redness Relief, Sterile recalledTarget Eye Drops Maximum Redness Relief Eye | K.C. Pharmaceuticals | Sterility | Nationwide |
| Drug | CLASS III | Tretinoin Cream UPS recalled by SUN Pharmaceutical IndustriesTretinoin | SUN Pharmaceutical Industries | Potency & Assay | Nationwide |
| Drug | CLASS II | Tirzepatide/cyanocobalamin 64/2 MG/ML Injectable recalled | Carolina Infusion | Sterility | Nationwide |
| Drug | CLASS II | Sterile High Performance Ultra Lubricating Eye Drops recalledLeader Ultra Lubricating Eye Drops | K.C. Pharmaceuticals | Sterility | Nationwide |
| Drug | CLASS II | Tirzepatide/cyanocobalamin 85/2 MG/ML Injectable recalled | Carolina Infusion | Sterility | Nationwide |
| Drug | CLASS III | Tretinoin Cream USP, 0.05% tube recalledTretinoin | SUN Pharmaceutical Industries | Potency & Assay | Nationwide |
| Drug | CLASS II | Tri-Mix (Papav/Phento/Alpros),30/2/20, injectable recalled | Carolina Infusion | Sterility | Nationwide |
| Drug | CLASS II | Lidocaine Ointment USP, 5% (Generic for Xylocaine) recalled | Preferred Pharmaceuticals | Packaging Defects | Nationwide |
| Drug | CLASS II | Tirzepatide Injection, 18mg/mL Sterile Multi-Dose Vial recalled | Apothecary Pharma | Sterility | Nationwide |
| Drug | CLASS II | Tri-Mix (Papav/Phento/Alpros), 30/1/40, injectable recalled | Carolina Infusion | Sterility | Nationwide |
| Drug | CLASS II | Sterile Eye Drops, Original recalled by K.C. PharmaceuticalsGoodsense Eye Drops Original Formula | K.C. Pharmaceuticals | Sterility | Nationwide |
| Drug | CLASS II | Imaavy (nipocalimab-aahu) Injection, 300 mg recalledImaavy | J&J Innovative Medicine | Particulate Matter | OH |
| Drug | CLASS II | Tri-Mix (Papav/Phento/Alpros),30/2/40 recalled by Carolina Infusion | Carolina Infusion | Sterility | Nationwide |
| Drug | CLASS II | Fosfomycin Tromethamine Granules for Oral Solution recalled by Cipla USAFosfomycin Tromethamine | Cipla USA | Potency & Assay | Nationwide |
| Drug | CLASS II | Sterile EYE Drops Advanced Relief, (dextran recalledLeader Advanced Relief Eye Drops | K.C. Pharmaceuticals | Sterility | Nationwide |
| Drug | CLASS II | Tri-Mix (Papav/Phento/Alpros),30/1/60, injectable recalled | Carolina Infusion | Sterility | Nationwide |
| Drug | CLASS II | Tri-Mix (Papav/Phento/Alpros),30/1/10, injectable recalled | Carolina Infusion | Sterility | Nationwide |
| Drug | CLASS II | Tri-Mix (Papav/Phento/Alpros),30/1/20, injectable recalled | Carolina Infusion | Sterility | Nationwide |
| Drug | CLASS II | Tirzepatide/cyanocobalamin 26/2 MG/ML Injectable recalled | Carolina Infusion | Sterility | Nationwide |
| Drug | CLASS II | Quad-mix( Papav/phento/alpros/trop) Injectable recalled | Carolina Infusion | Sterility | Nationwide |
| Drug | CLASS II | Sterile Lubricant Dry Eye Relief Eye Drops recalledLeader Dry Eye Relief Eye Drops | K.C. Pharmaceuticals | Sterility | Nationwide |
| Food | ANNOUNCED | Para Bien Al Grano recalled by Pan PepinPara Bien | Pan Pepin | Undeclared Sesame | PR |
| Food | CLASS II | Frozen Pepperoni Pizza recalled by Saint Francis Apizza | Saint Francis Apizza | Undeclared Soy | KY, OH |
| Food | CLASS II | Salsa Bean Dip Express Tray recalled by WinCo Foods | WinCo Foods | Foreign Material | 8 states |
| Food | CLASS II | Mezzetta Golden Greek Peperoncini Medium Heat G.L. Mezzetta recalledMezzetta | G L Mezzetta | Foreign Material | 22 states |
| Food | CLASS I | Alfalfa Sprouting Seeds recalled by Berlin SeedsAlfalfa Sprouting | Berlin Seeds | Salmonella | Nationwide |
| Food | CLASS II | Cranberry Chicken Salad Wedge package in Wedge recalledCranberry | Freshpoint Central Florida | Undeclared Allergens | FL, GA |
| Food | CLASS I | X10 Natural Enhancement Supplement, 7 sachets/box recalled | A&P Creations | Undeclared Allergens | Nationwide |
| Food | NOT YET CLASSIFIED | Graziers Raw Milk Sharp Cheddar recalled by Sierra Nevada CheeseGraziers | Sierra Nevada Cheese | E. coli | 13 states |
| Food | ANNOUNCED | Pan Pepín Inc. Emite Alerta por Alérgenos en el Producto recalled | | Other | |
| Food | ANNOUNCED | Starfish Seafood Cold Smoked Salmon recalled by Krasnyi OktyabrStarfish Seafood | Krasnyi Oktyabr | Listeria | 6 states |
| Food | ANNOUNCED | Starfish Seafood Cold Smoked Salmon, Halibut, and Trout recalledStarfish Seafood | Krasnyi Oktyabr | Listeria | 6 states |
| Food | ANNOUNCED | Riad's Oliva to Go Baba Ghanouj, Spicy Baba Ghanouj, and Hummus recalledRiad's Oliva to Go | Oliva | Undeclared Sesame | CT, MA |
| Drug | ANNOUNCED | Par Pharmaceutical Brevital Sodium 500 mg/vial for Injection recalledPar Pharmaceutical | Par Health | Particulate Matter | Nationwide |
| Food | CLASS I | Alfalfa Sprouting Seeds recalled by Todd's SeedsAlfalfa Sprouting | Todd's Seeds | Salmonella | Nationwide |
| Food | CLASS II | Organiccs Absolutely Pure, Type-1 Hydrolyzed Collagen recalledOrganiccs Absolutely | Pacific Health Sciences | Undeclared Fish & Shellfish | 6 states |
| Food | CLASS II | Cloud Cafe branded Collagen Milk recalled by TojiCloud Cafe | Toji | Undeclared Allergens | CA |
| Food | CLASS I | Sprouting Seed Mix - Broccoli, Radish, Alfalfa recalled by Todd's SeedsSprouting | Todd's Seeds | Salmonella | Nationwide |
| Food | CLASS II | Khazana The Treasure Spice Magic Fennel Candy recalled by SLT FoodsKhazana | SLT Foods | Undeclared Allergens | NY |
| Food | CLASS I | Alfalfa & Mung Bundle each), packaged separately recalledAlfalfa | Todd's Seeds | Salmonella | Nationwide |
| Food | CLASS I | Variety Pack of Sprouting Seeds - Broccoli, Alfalfa recalledVariety | Todd's Seeds | Salmonella | Nationwide |
| Food | CLASS I | Salata Salad Kitchen Jalapen¿o Avocado Dressing recalledSalata | Salata Dressings | Salmonella | GA, NC, TX |
| Food | CLASS I | Coco G's Courmet Flaming Cheddar Hots, Spicy Cheddar Cheese Popcorn recalledCoco G's | Coco G's Snack Foods | Salmonella | IL, WI |
| Food | CLASS I | Broccoli & Friends Sprouting Seed Mix - Broccoli, Alfalfa recalledBroccoli | Todd's Seeds | Salmonella | Nationwide |
| Food | CLASS II | 7up Tropical beverage, shelf stable can in a wrap recalled | Admiral Beverage | Undeclared Allergens | UT |
| Food | CLASS I | Salad Sprouting Mixture - Broccoli, Mustard, Alfalfa and Cabbage recalled | Todd's Seeds | Salmonella | Nationwide |
| Device | CLASS II | SmartPath to dStream for XR and 3.0T recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Hopkins Telescope 30¿ recalled by Karl Storz Endoscopy | Karl Storz Endoscopy | Packaging Defects | Nationwide |
| Device | CLASS II | Disposable Tourniquet Cuff, 24" X 4" 1-Line, Yellow recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Mpr Single Use Tourniquet Cuff 15" 1 Line recalled by ASP Global | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 12" X 3.5" 1-Line (CS Plum recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | NOxBOXi Nitric Oxide Delivery System recalled | Noxbox | Device Malfunction | Nationwide |
| Device | CLASS II | Palacos R pro recalled by Heraeus Medical GmbH (Dental | Heraeus Medical GmbH (Dental Division) | Packaging Defects | Nationwide |
| Device | CLASS II | Intrapulmonary Percussive Ventilation, IPV 1, Product Number: S00065 recalled | Percussionaire | Other | Nationwide |
| Device | CLASS II | Disposable Tourniquet Cuff, 44" X 4" 2-Line, Green recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 44" X 4" 2-Line (CS Green recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Fisher Scientific Sure-Vue Urine hCG Strip recalled by Alere San Diego | Alere San Diego | Potency & Assay | Nationwide |
| Device | CLASS II | Mpr Single Use Tourniquet Cuff 24" 2 Line recalled by ASP Global | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 34" X 4" 1-Line (CS Blue recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 24" X 4" 2-Line (CS Yellow recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Positron Emission Tomography and Computed Tomography System recalled | Shanghai United Imaging Healthcare | Device Malfunction | Nationwide |
| Device | CLASS II | Mpr Single Use Tourniquet Cuff 34" 2 Line recalled by ASP Global | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 12" X 3.5" 2-Line (CS Plum recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Disposable Tourniquet Cuff, 44" X 4" 1-Line, Green recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Upgrade to MR recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Mpr Disposable Tourniquet Cuff 18" 2 Line recalled by ASP Global | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Disposable Tourniquet Cuff, 24" X 4" 2-Line, Yellow recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 18" X 4" 1-Line (CS Red recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 34" X 4" 2-Line (CS Blue recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Intrapulmonary Percussive Ventilation, IPV-1C recalled by Percussionaire | Percussionaire | Other | Nationwide |
| Device | CLASS II | Opportunity Pro recalled by American Nitrile Operations | American Nitrile Operations | Device Malfunction | Nationwide |
| Device | CLASS II | Atellica CH Revised C-Reactive Protein (RCRP) recalled | Siemens Healthcare Diagnostics | Other | Nationwide |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 24" X 4" 2-Line (CS Yellow recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Positron Emission Tomography and Computed Tomography System recalled | Shanghai United Imaging Healthcare | Device Malfunction | Nationwide |
| Device | CLASS II | Mpr Single Use Tourniquet Cuff 8" 2 Line recalled by ASP Global | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Palacos R+G pro recalled by Heraeus Medical GmbH (Dental | Heraeus Medical GmbH (Dental Division) | Packaging Defects | Nationwide |
| Device | CLASS II | Palacos MV pro recalled by Heraeus Medical GmbH (Dental | Heraeus Medical GmbH (Dental Division) | Packaging Defects | Nationwide |
| Device | CLASS II | Medical convenience kits containing BD CliniClean Pericare recalled | American Contract Systems | Device Malfunction | Nationwide |
| Device | CLASS II | Tandem t:slim mobile application t:slim Mobile Application, iOS recalled | Tandem Diabetes Care | Device Malfunction | Nationwide |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 24" X 4" 1-Line (CS Yellow recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Presource Packs Containing Stryker StrykeFlow PS recalled | Cardinal Health 200 | Packaging Defects | Nationwide |
| Device | CLASS II | McKesson Consult hCG Urine Cassette recalled by Alere San Diego | Alere San Diego | Potency & Assay | Nationwide |
| Device | CLASS II | Travel Air, Product Number: S00055 recalled by Percussionaire | Percussionaire | Other | Nationwide |
| Device | CLASS II | Systems/units containing affected recalled | Beckman Coulter Mishima K.K | Device Malfunction | Nationwide |
| Device | CLASS II | Disposable Tourniquet Cuff, 34" X 4" 2-Line, Blue recalled by ASP Global | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Mpr Single Use Tourniquet Cuff 30" 1 Line recalled by ASP Global | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Mpr Single Use Tourniquet Cuff 12" 2 Line recalled by ASP Global | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Opportunity Flex recalled by American Nitrile Operations | American Nitrile Operations | Device Malfunction | Nationwide |
| Device | CLASS II | Olympus M3 Gold Autoclavable Lateral Telescope recalled | Olympus Corporation of the Americas | Sterility | PA |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 26" X 6" 1-Line (CS Orange recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 30" X 4" 2-Line (CS White recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 34" X 4" 1-Line (CS Blue recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Mpr Single Use Tourniquet Cuff 30" 2 Line recalled by ASP Global | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Ingenia Elition S and Ingenia Elition recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 8" X 2.5" 2-Line (CS recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Computed Tomography X-ray System recalled by Shanghai United Imaging | Shanghai United Imaging Healthcare | Device Malfunction | Nationwide |
| Device | CLASS II | Positron Emission Tomography and Computed Tomography System recalled | Shanghai United Imaging Healthcare | Device Malfunction | Nationwide |
| Device | CLASS II | Olympus Tripp-Lite P580-025 25ft DisplayPort Cable recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS II | Mpr Single Use Tourniquet Cuff 44" 1 Line recalled by ASP Global | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Mpr Single Use Tourniquet Cuff 15" 2 Line recalled by ASP Global | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Charlotte Claw Screw recalled by Wright Medical Technology | Wright Medical Technology | Other | Nationwide |
| Device | CLASS II | Positron Emission Tomography and Computed Tomography System recalled | Shanghai United Imaging Healthcare | Device Malfunction | Nationwide |
| Device | CLASS II | Disposable Tourniquet Cuff, 30" X 4" 2-Line, White recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Presource Packs Containing Stryker StrykeFlow PS recalled | Cardinal Health 200 | Packaging Defects | Nationwide |
| Device | CLASS II | Disposable Tourniquet Cuff, 18" X 4" 1-Line, Red recalled by ASP Global | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 8" X 2.5" 1-Line recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Ingenia Ambition S and Ingenia Ambition recalled | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 12" X 3.5" 2-Line (CS Plum recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 15" X 4" 1-Line (CS Gray recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 15" X 4" 2-Line (CS Gray recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Ingenia Blue Seal SE and Blue Seal XE recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Computed Tomography X-ray System recalled by Shanghai United Imaging | Shanghai United Imaging Healthcare | Device Malfunction | Nationwide |
| Device | CLASS II | Palacos MV+G pro recalled by Heraeus Medical GmbH (Dental | Heraeus Medical GmbH (Dental Division) | Packaging Defects | Nationwide |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 34" X 4" 2-Line (CS Blue recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Fisher Scientific Sure-Vue Urine hCG recalled by Alere San Diego | Alere San Diego | Potency & Assay | Nationwide |
| Device | CLASS II | SmartPath to MR recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | MR 5300; Model number (REF): 1. 782110, 2. 782152 recalled | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Mpr Single Use Tourniquet Cuff 24" 1 Line recalled by ASP Global | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 44" X 4" 1-Line (CS Green recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Medical convenience kits containing BD CliniClean Pericare recalled | American Contract Systems | Device Malfunction | Nationwide |
| Device | CLASS II | Mpr Disposable Tourniquet Cuff 20" Dual Bladder, 1 Line recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | EnCor EnCompass Breast Biopsy and Tissue Removal System Console recalled | Bard Peripheral Vascular | Device Malfunction | Nationwide |
| Device | CLASS II | Mpr Single Use Tourniquet Cuff 34" 1 Line recalled by ASP Global | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 44" X 4" 2-Line (CS Green recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Mpr Disposable Tourniquet Cuff 20" Dual Bladder, 2 Line recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Pipeline Flex Embolization Device with Shield Technology recalled | Micro Therapeutics | Labeling Errors | Nationwide |
| Device | CLASS II | Olympus M3 Gold Autoclavable Foroblique Telescope recalled | Olympus Corporation of the Americas | Sterility | PA |
| Device | CLASS II | Impulsator, Product Number: S00010, Phasitron recalled by Percussionaire | Percussionaire | Other | Nationwide |
| Device | CLASS II | Mpr Single Use Tourniquet Cuff 12" 1 Line recalled by ASP Global | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 15" X 4" 2-Line (CS Gray recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Disposable Tourniquet Cuff, 30" X 4" 1-Line, White recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | NovaSeq 6000Dx including Dragen Server recalled by Illumina | Illumina | Potency & Assay | Nationwide |
| Device | CLASS II | Expressaire Disposable BB Tournquet Cuff recalled by ASP Global | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | In-Line Valve, Product Number: P5-TEE recalled by Percussionaire | Percussionaire | Other | Nationwide |
| Device | CLASS II | Mpr Single Use Tourniquet Cuff 18" 1 Line recalled by ASP Global | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 18" X 4" 1-Line (CS Red recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Mpr Single Use Tourniquet Cuff 26" Dual Bladder, 2 Line recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Upgrade dStream recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS I | VentStar Resus Neo recalled by Draeger | Draeger | Packaging Defects | Nationwide |
| Device | CLASS II | Fisher Scientific Sure-Vue Serum/Urine hCG recalled by Alere San Diego | Alere San Diego | Potency & Assay | Nationwide |
| Device | CLASS II | Computed Tomography X-ray System recalled by Shanghai United Imaging | Shanghai United Imaging Healthcare | Device Malfunction | Nationwide |
| Device | CLASS II | Computed Tomography X-ray System recalled by Shanghai United Imaging | Shanghai United Imaging Healthcare | Device Malfunction | Nationwide |
| Device | CLASS II | Positron Emission Tomography and Computed Tomography System recalled | Shanghai United Imaging Healthcare | Device Malfunction | Nationwide |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 44" X 4" 1-Line (CS Green recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Philips Medical Systems Technologies Ltd recalled | Philips North America | Device Malfunction | MA |
| Device | CLASS II | Disposable Tourniquet Cuff, 18" X 4" 2-Line, Red recalled by ASP Global | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 38" X 4" 1-Line (CS recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 18" X 4" 2-Line (CS Red recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Presource Packs Containing Stryker StrykeFlow PS recalled | Cardinal Health 200 | Packaging Defects | Nationwide |
| Device | CLASS II | Evolution upgrade 1.5T amd Evolution upgrade 3.0T recalled | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Positron Emission Tomography and Computed Tomography System recalled | Shanghai United Imaging Healthcare | Device Malfunction | Nationwide |
| Device | CLASS II | Disposable Tourniquet Cuff, 34" X 4" 1-Line, Blue recalled by ASP Global | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Computed Tomography X-ray System recalled by Shanghai United Imaging | Shanghai United Imaging Healthcare | Device Malfunction | Nationwide |
| Device | CLASS II | Ingenia 1.5T, 1.5T CX, and 1.5T recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Expressaire Disposable BB Tournquet Cuff recalled by ASP Global | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | System (RED 62 Reperfusion Catheter) recalled by Penumbra | Penumbra | Device Malfunction | Nationwide |
| Device | CLASS I | Medline Basic Homecare Beds and Medlite Homecare Beds recalled | Medline Industries | Device Malfunction | Nationwide |
| Device | CLASS II | Performance Pro recalled by American Nitrile Operations | American Nitrile Operations | Device Malfunction | Nationwide |
| Device | CLASS II | Intrapulmonary Percussive Ventilation, IPV-2C recalled by Percussionaire | Percussionaire | Other | Nationwide |
| Device | CLASS II | Ferndale Laboratories recalled by Custom Interventional Pain | Custom Interventional Pain Management | Foreign Material | Nationwide |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 24" X 4" 1-Line (CS Yellow recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Philips IntraSight Plus recalled by Volcano | Volcano | Device Malfunction | Nationwide |
| Device | CLASS II | Medical convenience kits containing BD CliniClean Pericare recalled | American Contract Systems | Device Malfunction | Nationwide |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 30" X 4" 1-Line (CS White recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Disposable Tourniquet Cuff, 12" X 3.5" 2-Line, Plum recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 18" X 4" 2-Line (CS Red recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 30" X 4" 1-Line (CS White recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Quantum PureFlow Standard Heat Exchanger High Flow 3/8 recalled | Spectrum Medical | Packaging Defects | Nationwide |
| Device | CLASS II | Presource Packs Containing Stryker StrykeFlow PS recalled | Cardinal Health 200 | Packaging Defects | Nationwide |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 20" X 6" 1-Line recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | MR 7700; Model number (REF): 1. 782120, 2. 782153 recalled | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Mpr Single Use Tourniquet Cuff 44" 2 Line recalled by ASP Global | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Intrapulmonary Percussive Ventilation, IPV HC recalled by Percussionaire | Percussionaire | Other | Nationwide |
| Device | CLASS II | Computed Tomography X-ray System recalled by Shanghai United Imaging | Shanghai United Imaging Healthcare | Device Malfunction | Nationwide |
| Device | CLASS II | Embosphere 500-700 micrometer Syringe Sterile Steam recalled | Merit Medical Systems | Sterility | Nationwide |
| Device | CLASS II | Quantum PureFlow Standard Heat Exchanger High Flow 3/8 recalled | Spectrum Medical | Packaging Defects | Nationwide |
| Device | CLASS II | Expressaire Disposable BB Tournquet Cuff recalled by ASP Global | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 8" X 2.5" 2-Line recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Ingenia 3.0T and 3.0T CX recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS I | Medline Basic Homecare Beds and Medlite Homecare Beds recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 30" X 4" 2-Line (CS White recalled | ASP Global | Device Malfunction | Nationwide |
| Drug | CLASS II | Ranolazine Extended-Release Tablets, 1000 mg recalledRanolazine | Ajanta Pharma USA | Potency & Assay | Nationwide |
| Drug | CLASS II | Buprenorphine Hydrochloride, Injection 0.3 mg/mL recalledBuprenorphine Hydrochloride | Par Health USA | Other | Nationwide |
| Drug | CLASS II | Benzoyl Peroxide Wash recalled by SV Labs Toronto | SV Labs Toronto | Sterility | IL |
| Drug | CLASS II | Paroxetine Extended-Release Tablets, 37.5mg recalled by ApotexParoxetine Hydrochloride | Apotex | Potency & Assay | Nationwide |
| Drug | CLASS II | Zoladex (goserelin) implant, 3.6 mg, One single-Use Syringe recalledZoladex | TerSera Therapeutics | Temperature Abuse | Nationwide |
| Drug | CLASS II | Focus PI Hypromellose 0.7% Formula, 0.3 FL O per vial, Sterile recalledFocus Pi | Aurolab Trust | Sterility | VA |
| Drug | CLASS II | Estradiol Gel, 0.1%, 0.25 mg, 30-packets recalledEstradiol | Amneal Pharmaceuticals | Other | Nationwide |
| Drug | CLASS II | Benzoyl Peroxide Wash recalled by SV Labs Toronto | SV Labs Toronto | Sterility | IL |
| Food | ANNOUNCED | Broccoli Seeds - Calabrese recalled by Eden BrothersEDEN BROTHERS | Eden Brothers | Salmonella | Nationwide |
| Food | ANNOUNCED | Rapture Preworkout Dietary Supplement Powder recalled by Leader FormulasRAPTURE | Leader Formulas | Hidden Drug Ingredients | Nationwide |
| Food | CLASS II | Lior Cinnamon Ground Seasoning recalled by Galil ImportingLior Cinnamon | Galil Importing | Lead & Heavy Metals | 6 states |
| Food | CLASS II | Kofinas Garlic Mediterranean Infused Extra Virgin Olive Oil recalledKofinas Garlic | Lmsi | Hidden Drug Ingredients | 13 states |
| Food | HEALTH ALERT | Ineligible Chicken Vienna-Style Sausage Products Illegally recalled | FSIS | Processing Deviation | |
| Device | ANNOUNCED | StatStrip Glucose Hospital Meter System recalled by Nova BiomedicalNova Biomedical StatStrip | Nova Biomedical | Device Malfunction | |
| Food | ANNOUNCED | Nature's Own Hawaiian Bread single loaf recalled by Flowers FoodsNature's Own | Flowers Foods | Undeclared Milk | 5 states |
| Food | CLASS I | Ineligible Pork Cracklings Products recalled by Inexport Logistics | Inexport Logistics | Processing Deviation | |
| Food | ANNOUNCED | Great Value, Trader Joe’s Organic Blueberries recalledGreat Value, Trader Joe’s | Frutas y Hortalizas del Sur | E. coli | 35 states |
| Food | ANNOUNCED | Ice cream recalled by Stewart’s ShopStewart’s Shops | Stewart’s Shop | Foreign Material | NH, NY, VT |
| Food | ANNOUNCED | Bettergoods Pasta recalled by Gias FoodsBettergoods | Gias Foods | Listeria | Nationwide |