| Device | CLASS II | Olympus Thunderbeat, Front-Actuated Grip recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS II | Olympus Thunderbeat Inline Grip recalled by Olympus Corporation of the | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS II | Medline Convenience Kits: Scc RF Pain Mgmt recalled | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Medline Convenience Kits: Drape Pack recalled by Medline Industries | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Olympus Thunderbeat, Inline Grip recalled by Olympus Corporation of the | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS II | Olympus Thunderbeat Front-Actuated Grip recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS II | Olympus Thunderbeat, Front-Actuated Grip Type S recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS II | Prodisc C SK recalled by Centinel Spine | Centinel Spine | Labeling Errors | Nationwide |
| Device | CLASS II | Medline Convenience Kits: Chest/Breast-lf recalled by Medline Industries | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Medline Convenience Kits: Kit Urology Sling recalled | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Medline Convenience Kits: C-section Pack recalled by Medline Industries | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Medline Convenience Kits: OR Arteriogram recalled by Medline Industries | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Medline Convenience Kits: Basic Nerve Block Tray W/Linen recalled | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Da Vinci 5 Assy, DV5 Console, IS5000 recalled by Intuitive Surgical | Intuitive Surgical | Device Malfunction | 6 states |
| Device | CLASS II | Medline Convenience Kits: Arthroscopy CDS recalled by Medline Industries | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Medline Convenience Kits: Hysteroscopy recalled by Medline Industries | Medline Industries | Sterility | Nationwide |
| Device | CLASS I | Olympus High Flow Insufflation Unit recalled | Olympus Corporation of the Americas | Device Malfunction | Nationwide |
| Device | CLASS II | Medline Convenience Kits: Kit Ophthalmic Rupture Globe recalled | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Medline Convenience Kits: Dental Pack recalled by Medline Industries | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Medihoney Calcium Alginate With Active Leptospermum Honey recalled | Integra LifeSciences Corp. (NeuroSciences) | Sterility | Nationwide |
| Device | CLASS II | Medline Convenience Kits: PICC Line Tray recalled by Medline Industries | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Capillary Tubes recalled by Medica | Medica | Other | MA |
| Device | CLASS II | Medline Surgical Packs: Pack,Universal,Ultragard,5/CS recalled | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Medline Convenience Kits: Tote Abrams Knee Arthroscopy recalled | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Molli 2 System includes: MM1000 (Pack recalled by Stryker | Stryker | Other | Nationwide |
| Device | CLASS II | Medline Convenience Kits: OB KIT recalled by Medline Industries | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Medline Convenience Kits: Endo Kit W/Syringe recalled | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Olympus Thunderbeat, Inline Grip recalled by Olympus Corporation of the | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS II | Olympus Thunderbeat, Pistol Grip recalled by Olympus Corporation of the | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS II | Medline Convenience Kits: Neuro Shunt- Codman recalled | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Medline Convenience Kits: Plastic Bin W/Misc Kits recalled | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Olympus Thunderbeat, Front-Actuated Grip recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS II | Medline Convenience Kits: Baptist Floyd Endo GI Kit recalled | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Medline Convenience Kits: Burn Pack recalled by Medline Industries | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Medline Convenience Kits: Robotic GYN recalled by Medline Industries | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Spectrum IQ Infusion Pump recalled by Baxter Healthcare | Baxter Healthcare | Device Malfunction | OH |
| Device | CLASS II | Medline Convenience Kits: WMC I D Pack-lf recalled by Medline Industries | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Medline Convenience Kits: Ancillary Pack-lf recalled | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Medline Convenience Kits: Lvad Driveline Tray recalled | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Medline Convenience Kits: PPE KIT recalled by Medline Industries | Medline Industries | Sterility | Nationwide |
| Device | CLASS I | Olympus High Flow Insufflation Unit recalled | Olympus Corporation of the Americas | Device Malfunction | Nationwide |
| Device | CLASS II | Medline Convenience Kits: Lithotomy Pack recalled by Medline Industries | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Medline Convenience Kits: Chp Cochlear Supplement Cds recalled | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Medline Convenience Kits: KIT STC Tracheostomy recalled | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Medline Convenience Kits: Kit General Closure recalled | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Olympus Thunderbeat, Inline Grip recalled by Olympus Corporation of the | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS I | Olympus High Flow Insufflation Unit recalled | Olympus Corporation of the Americas | Device Malfunction | Nationwide |
| Device | CLASS II | Private Label CVS recalled by Integra LifeSciences Corp. | Integra LifeSciences Corp. (NeuroSciences) | Sterility | Nationwide |
| Device | CLASS II | Medline Convenience Kits: Bap North Robotic Surgery Cds recalled | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Olympus Thunderbeat, Front-Actuated Grip Type S recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS II | Monarch Platform, Bronchoscopy recalled by Auris Health | Auris Health | Device Malfunction | Nationwide |
| Device | CLASS II | Teslatome Bipolar Sphincterotomes recalled by Wilson-Cook Medical | Wilson-Cook Medical | Other | 4 states |
| Device | CLASS II | IV Administration and Extension Sets recalled by Medline Industries | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | Medline Convenience Kits: Admit KIT recalled by Medline Industries | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Medline Convenience Kits: Lvad Driveline Tray recalled | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Olympus Thunderbeat, Pistol Grip recalled by Olympus Corporation of the | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS II | Medline Convenience Kits: Drape Pack-choice recalled | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Olympus Thunderbeat, Front-Actuated Grip Type S recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS II | Medline Convenience Kits: Kit Aces Insert Peg recalled | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | MediHoney Gel with Active Leptospermum Honey recalled | Integra LifeSciences Corp. (NeuroSciences) | Sterility | Nationwide |
| Device | CLASS II | Broviac 4. Single-Lumen CV Catheter Cutdown Tray recalled | Bard Peripheral Vascular | Sterility | Nationwide |
| Device | CLASS II | Medline Convenience Kits: Kit Triple Lumen Insertion recalled | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Estrone RIA recalled by Immunotech A.S | Immunotech A.S | Other | Nationwide |
| Device | CLASS II | Medline Convenience Kits: Kit Surg Onc Excision Breast recalled | Medline Industries | Sterility | Nationwide |
| Food | CLASS II | Woodland Gourmet Arrowroot Flour recalledWoodland | Woodland Foods | Foreign Material | KY |
| Food | CLASS II | Brass Tope. Sticker label: $29.99+TAX recalled by Lotus MomBrass Tope | Lotus Mom | Lead & Heavy Metals | CA, CO |
| Food | CLASS II | IKM Aluminum Saucepan 9" with Wooden Handle recalled by Lotus MomIKM Aluminum | Lotus Mom | Lead & Heavy Metals | CA, CO |
| Food | CLASS II | Frozen Cooked Medium Shrimp Peeled & Deveined, Tail Off-White Shrimp recalled | H & N Group | Foreign Material | CA |
| Food | CLASS I | The Tuna Salad product container is mislabeled recalled | Reser's Fine Foods | Undeclared Fish & Shellfish | 5 states |
| Food | CLASS II | Pure Factors Professional Nighttime Sleep Formula recalled | Pure Solutions | Undeclared Milk | 36 states |
| Food | CLASS I | Why Not Natural Moringa Capsules bottle marked recalled by Art MonkeyWhy Not | Art Monkey | Salmonella | Nationwide |
| Food | CLASS II | Aluminum Kadai with Metal Handles Size A-Cook recalled by Lotus MomAluminum Kadai | Lotus Mom | Lead & Heavy Metals | CA, CO |
| Food | CLASS I | Brass Pital Pot Sticker label: Brass Hammered Handi NO recalledBrass Pital | Lotus Mom | Lead & Heavy Metals | CA, CO |
| Food | CLASS I | Ready-To-Eat Frozen Meatball Products recalled by Rosina Food Products | Rosina Food Products | Foreign Material | |
| Food | CLASS I | Siluriformes Fish Products recalled by Sobico USA | Sobico USA | Packaging Defects | |
| Food | CLASS I | Chicken Fried Rice Products recalled by Ajinomoto Foods North America | Ajinomoto Foods North America | Foreign Material | |
| Device | CLASS II | Spectral CT 7500 on Rails recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Medline medical convenience kits packaged as recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS I | Medline ReNewal Reprocessed ViewFlex Xtra ICE Catheters recalled | Medline Industries | Particulate Matter | Nationwide |
| Device | CLASS II | Medline medical convenience kits packaged as recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | Medline medical convenience kits packaged as recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS I | Reprocessed Livewire Steerable Diagnostic Electrophysiology recalled | Medline Industries | Particulate Matter | Nationwide |
| Device | CLASS II | Universal KIT, Kit recalled by Medline Industries | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | Medline medical convenience kits packaged as recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS I | Reprocessed Biosense Webster Soundstar eco Diagnostic recalled | Medline Industries | Particulate Matter | Nationwide |
| Device | CLASS II | Brevera Breast Biopsy System Disposable Needle recalled by Hologic | Hologic | Particulate Matter | Nationwide |
| Device | CLASS II | Medline medical convenience kits packaged as recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | Atec Lateral Navigation Disc Prep Instruments Lif Nav, Osteotome recalled | Alphatec Spine | Packaging Defects | Nationwide |
| Device | CLASS III | Surepulse VS Cap Extra Large recalled by Surepulse Medical | Surepulse Medical | Other | Nationwide |
| Device | CLASS II | Intubation Tray (Adult) containing Suction Catheter Kits recalled | Medline Industries | Device Malfunction | Nationwide |
| Device | CLASS III | Surepulse VS Cap Extra Small recalled by Surepulse Medical | Surepulse Medical | Other | Nationwide |
| Device | CLASS II | Azurion 5 M20 System recalled by Philips Medical Systems | Philips Medical Systems Nederl | Device Malfunction | Nationwide |
| Device | CLASS II | Leksell GammaPlan Radionuclide RT Treatment planning system recalled | Elekta | Device Malfunction | Nationwide |
| Device | CLASS II | Medline medical convenience kits packaged as recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | Barco MNA with the HexaVue IP Integration System recalled by Steris | Steris | Other | Nationwide |
| Device | CLASS II | Azurion 7 B20 System recalled by Philips Medical Systems | Philips Medical Systems Nederl | Device Malfunction | Nationwide |
| Device | CLASS II | Medline medical convenience kits packaged as recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS III | Surepulse VS Cap Small recalled by Surepulse Medical | Surepulse Medical | Other | Nationwide |
| Device | CLASS II | Medline medical convenience kits packaged as recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | Azurion 3 M12 System recalled by Philips Medical Systems | Philips Medical Systems Nederl | Device Malfunction | Nationwide |
| Device | CLASS I | Reprocessed St. Jude Supreme recalled by Medline Industries | Medline Industries | Particulate Matter | Nationwide |
| Device | CLASS III | WB Impression Post Closed Tray incl recalled by Straumann USA | Straumann USA | Packaging Defects | Nationwide |
| Device | CLASS II | Atec Lateral Navigation Disc Prep Instruments Lif Nav, Osteotome recalled | Alphatec Spine | Packaging Defects | Nationwide |
| Device | CLASS II | IQon Spectral CT recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Azurion 3 M15 System recalled by Philips Medical Systems | Philips Medical Systems Nederl | Device Malfunction | Nationwide |
| Device | CLASS II | Halyard Transport BAG KIT recalled by AVID Medical | Avid Medical | Sterility | Nationwide |
| Device | CLASS II | Azurion 5 M12 System recalled by Philips Medical Systems | Philips Medical Systems Nederl | Device Malfunction | Nationwide |
| Device | CLASS II | Medline medical convenience kits packaged as recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | da Vinci 5 Surgeon Console Viewer Display, Assy, DV5 Console, IS5000 recalled | Intuitive Surgical | Other | Nationwide |
| Device | CLASS II | Laerdal Compact Suction Unit 4 RTCA recalled by Laerdal Medical | Laerdal Medical | Other | Nationwide |
| Device | CLASS I | Reprocessed Siemens Acuson AcuNav Diagnostic Ultrasound recalled | Medline Industries | Particulate Matter | Nationwide |
| Device | CLASS II | Azurion 7 B12 System recalled by Philips Medical Systems | Philips Medical Systems Nederl | Device Malfunction | Nationwide |
| Device | CLASS I | Medline ReNewal Reprocessed Webster CS Catheters recalled | Medline Industries | Particulate Matter | Nationwide |
| Device | CLASS II | Azurion 7 M20 System recalled by Philips Medical Systems | Philips Medical Systems Nederl | Device Malfunction | Nationwide |
| Device | CLASS II | Medline Suction Catheter Kits recalled by Medline Industries | Medline Industries | Device Malfunction | Nationwide |
| Device | CLASS II | Azurion 7 M12 System recalled by Philips Medical Systems | Philips Medical Systems Nederl | Device Malfunction | Nationwide |
| Device | CLASS I | Reprocessed Abbott Inquiry Steerable Diagnostic Catheters recalled | Medline Industries | Particulate Matter | Nationwide |
| Device | CLASS II | Spectral CT recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Brilliance iCT recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS III | Surepulse VS Cap Medium recalled by Surepulse Medical | Surepulse Medical | Other | Nationwide |
| Device | CLASS II | Medline medical convenience kits packaged as recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS III | Surepulse VS Cap Large recalled by Surepulse Medical | Surepulse Medical | Other | Nationwide |
| Device | CLASS II | Leksell GammaPlan Radionuclide RT Treatment planning system recalled | Elekta | Device Malfunction | Nationwide |
| Drug | CLASS II | Estradiol, 6 mg, 1 Sterile Pellet recalled by F.H. INVESTMENTS, Inc. ( | F.H. Investments Inc. ( | Particulate Matter | Nationwide |
| Drug | CLASS II | Testosterone 75mg, Anastrozole 4mg, 1 Sterile Pellet recalled | F.H. Investments Inc. ( | Particulate Matter | Nationwide |
| Drug | CLASS II | Testosterone 100mg Anastrozole 4mg , 1 Sterile Pellet recalled | F.H. Investments Inc. ( | Particulate Matter | Nationwide |
| Drug | CLASS II | Estradiol, 22 mg, 1 Sterile Pellet recalled by F.H. INVESTMENTS, Inc. ( | F.H. Investments Inc. ( | Particulate Matter | Nationwide |
| Drug | CLASS II | For Sensitive Skin, 4% Lidocaine, [ or] recalledPro Numb Sensitive Skin | Pro Numb Tattoo Numbing Spray | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Testosterone 87.5mg, Triamcinolone Acetonide17.5 mcg recalled | F.H. Investments Inc. ( | Particulate Matter | Nationwide |
| Drug | CLASS II | Estradiol, 18 mg, 1 Sterile Pellet recalled by F.H. INVESTMENTS, Inc. ( | F.H. Investments Inc. ( | Particulate Matter | Nationwide |
| Drug | CLASS II | Testosterone, 37.5 mg, 1 Sterile Pellet recalled | F.H. Investments Inc. ( | Particulate Matter | Nationwide |
| Drug | CLASS II | Cetrorelix Acetate for Injection , 0.25 mg per vial, Single-Dose Kit recalled | Meitheal Pharmaceuticals | Other | Nationwide |
| Drug | CLASS II | Testosterone, 50.0 mg, 1 Sterile Pellet recalled | F.H. Investments Inc. ( | Particulate Matter | Nationwide |
| Drug | CLASS II | Estradiol,15 mg, 1 Sterile Pellet recalled by F.H. INVESTMENTS, Inc. ( | F.H. Investments Inc. ( | Particulate Matter | Nationwide |
| Drug | CLASS II | Testosterone, 18.0 mg, 1 Sterile Pellet recalled | F.H. Investments Inc. ( | Particulate Matter | Nationwide |
| Drug | CLASS II | acyclovir sodium, 200 mg, 200mg added recalled | Fresenius Kabi Compounding | Sterility | Nationwide |
| Drug | CLASS II | Estradiol, 12.5 mg, 1 Sterile Pellet recalled | F.H. Investments Inc. ( | Particulate Matter | Nationwide |
| Drug | CLASS II | Estradiol, 37.5 mg, 1 Sterile Pellet recalled | F.H. Investments Inc. ( | Particulate Matter | Nationwide |
| Drug | CLASS II | Testosterone 100mg, Triamcinolone Acetonide 20mcg recalled | F.H. Investments Inc. ( | Particulate Matter | Nationwide |
| Drug | CLASS II | Testosterone, 303 mg, 1 Sterile Pellet recalled | F.H. Investments Inc. ( | Particulate Matter | Nationwide |
| Drug | CLASS II | Testosterone 100mg, Anastrozole 4mg (4.5), 1 Sterile Pellet recalled | F.H. Investments Inc. ( | Particulate Matter | Nationwide |
| Drug | CLASS II | Testosterone, 12.5 mg, 1 Sterile Pellet recalled | F.H. Investments Inc. ( | Particulate Matter | Nationwide |
| Drug | CLASS III | Doxazosin Tablets, USP, 4 mg recalled by Unichem Pharmaceuticals USADoxazosin Mesylate | Unichem Pharmaceuticals USA | Other | Nationwide |
| Drug | CLASS II | Testosterone, 62.5 mg, 1 Sterile Pellet recalled | F.H. Investments Inc. ( | Particulate Matter | Nationwide |
| Drug | CLASS II | Estradiol, 20 mg, 1 Sterile Pellet recalled by F.H. INVESTMENTS, Inc. ( | F.H. Investments Inc. ( | Particulate Matter | Nationwide |
| Drug | CLASS II | vancomycin HCl added to, 0.9% Sodium Chloride Injection recalled | Fresenius Kabi Compounding | Sterility | Nationwide |
| Drug | CLASS II | Testosterone 200mg, Triamcinolone Acetonide 40mcg recalled | F.H. Investments Inc. ( | Particulate Matter | Nationwide |
| Drug | CLASS II | Estradiol, 10 mg, 1 Sterile Pellet recalled by F.H. INVESTMENTS, Inc. ( | F.H. Investments Inc. ( | Particulate Matter | Nationwide |
| Drug | CLASS II | Testosterone, 87.5 mg, 1 Sterile Pellet recalled | F.H. Investments Inc. ( | Particulate Matter | Nationwide |
| Drug | CLASS II | vancomycin HCl added to, 0.9% Sodium Chloride Injection recalled | Fresenius Kabi Compounding | Sterility | Nationwide |
| Drug | CLASS II | Estradiol, 25 mg, 1 Sterile Pellet recalled by F.H. INVESTMENTS, Inc. ( | F.H. Investments Inc. ( | Particulate Matter | Nationwide |
| Drug | CLASS II | Testosterone, 25.0 mg, 1 Sterile Pellet recalled | F.H. Investments Inc. ( | Particulate Matter | Nationwide |
| Drug | CLASS II | Testosterone, 200 mg, 1 Sterile Pellet recalled | F.H. Investments Inc. ( | Particulate Matter | Nationwide |
| Drug | CLASS II | Oxycodone Hydrochloride Tablets, USP (CII), 5 mg recalledOxycodone Hydrochloride | Amerisource Health Services | Packaging Defects | Nationwide |
| Drug | CLASS II | ketamine HCl, 1,000 mg, 1,000 mg per (10 mg per mL) recalled | Fresenius Kabi Compounding | Sterility | Nationwide |
| Drug | CLASS II | thiamine HCl, 500 mg, 500 mg added recalled | Fresenius Kabi Compounding | Sterility | Nationwide |
| Drug | CLASS II | 5% Lidocaine, [ or] recalled by Pro Numb Tattoo Numbing SprayPro Numb | Pro Numb Tattoo Numbing Spray | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Testosterone, 100 mg, 1 Sterile Pellet recalled | F.H. Investments Inc. ( | Particulate Matter | Nationwide |
| Drug | CLASS I | Udenyca, pegfilgrastim-cbqv injection recalled by McKessonUdenyca | McKesson | Temperature Abuse | Nationwide |
| Food | CLASS I | White Truffle Hummus recalled by Carrot Top Kitchens | Carrot Top Kitchens | Undeclared Sesame | NY |
| Food | CLASS II | Creamy Peanut Butter recalled by Ventura FoodsCreamy | Ventura Foods | Foreign Material | 40 states |
| Food | CLASS II | Karison Punjabi Pinni recalled by Karison Foods & SnacksKarison | Karison Foods & Snacks | Undeclared Milk | NJ, NY, VA |
| Food | CLASS II | Karison NO Sugar Added Besan Laddoo recalled by Karison Foods & SnacksKarison | Karison Foods & Snacks | Undeclared Milk | NJ, NY, VA |
| Food | CLASS I | Kirkland Signature Costco recalled by Costco WholesaleKirkland Signature | Costco Wholesale | Undeclared Tree Nuts | 24 states |
| Food | CLASS II | Ore-Ida Tater Tots shaped potatoes recalled by McCain Foods USAOre-Ida Tater | McCain Foods USA | Foreign Material | 28 states |
| Food | CLASS II | Karison Alsi Pinni recalled by Karison Foods & SnacksKarison | Karison Foods & Snacks | Undeclared Milk | NJ, NY, VA |
| Food | CLASS III | Sodexo Stars Saccharin (Pink) Packets, Sugar Substitute recalledSodexo Stars | Domino Foods | Undeclared Allergens | 14 states |
| Food | CLASS II | Brand: Red Button Movie House Popcorn Pack Size recalled | Lee's Commissary | Foreign Material | 8 states |
| Food | CLASS I | Lemon & Garlic Hummus recalled by Carrot Top Kitchens | Carrot Top Kitchens | Undeclared Sesame | NY |
| Food | CLASS II | Sonic Tots recalled by McCain Foods USASonic Tots | McCain Foods USA | Foreign Material | 28 states |
| Food | CLASS II | Karison Besan Laddoo recalled by Karison Foods & SnacksKarison | Karison Foods & Snacks | Undeclared Milk | NJ, NY, VA |
| Food | CLASS II | Smoked Grouper Dip with tamper proof lid tub recalled by Island Crab | Island Crab | Undeclared Milk | FL |
| Food | CLASS II | Creamy Peanut Butter recalled by Ventura FoodsCreamy | Ventura Foods | Foreign Material | 40 states |
| Food | CLASS II | Aonic Complete His recalled by TKS Co-pack ManufacturingAonic Complete | TKS Co-pack Manufacturing | E. coli | UT |
| Food | CLASS I | Sundried Tomato and Caper Hummus recalled by Carrot Top Kitchens | Carrot Top Kitchens | Undeclared Sesame | NY |
| Food | CLASS II | Creamy Peanut Butter recalled by Ventura FoodsCreamy | Ventura Foods | Foreign Material | 40 states |
| Food | CLASS I | Cherry Pepper Hummus recalled by Carrot Top Kitchens | Carrot Top Kitchens | Undeclared Sesame | NY |
| Food | CLASS II | Karison Panjiri recalled by Karison Foods & SnacksKarison | Karison Foods & Snacks | Undeclared Milk | NJ, NY, VA |
| Food | CLASS I | Lime Ginger Hummus recalled by Carrot Top Kitchens | Carrot Top Kitchens | Undeclared Sesame | NY |
| Food | CLASS II | Aonic Complete Hers recalled by TKS Co-pack ManufacturingAonic Complete | TKS Co-pack Manufacturing | E. coli | UT |
| Food | CLASS II | Crunchy Caramel artisan dark chocolate recalled by Cacao ArtCrunchy Caramel | Cacao Art | Undeclared Milk | FL |
| Food | CLASS II | a.) Preema brand Bright Red Food Colour Powder recalled by KPCM New YorkPreema | KPCM New York | Undeclared Allergens | MA, NY |
| Food | CLASS II | Spicy Breakfast Burrito in a flour tortilla recalled | MG Foods-Compass Group | Foreign Material | 7 states |
| Device | CLASS II | Vivoo Vaginal pH Test recalled by Changchun Wancheng | Changchun Wancheng Bio-Electron | Labeling Errors | Nationwide |
| Device | CLASS II | Lindsell Sutured IOL Marker, VS0390 - Scleral Marker recalled | Vortex Surgical | Sterility | Nationwide |
| Device | CLASS II | Menopause Test Cassette (Urine) recalled by Changchun Wancheng | Changchun Wancheng Bio-Electron | Labeling Errors | Nationwide |
| Device | CLASS II | da Vinci X, Xi Surgical System, & da Vinci 5 Surgical System recalled | Intuitive Surgical | Device Malfunction | 30 states |
| Device | CLASS II | Lumipulse G pTau 217 Plasma Immunoreaction Cartridges recalled | Fujirebio Diagnostics | Labeling Errors | Nationwide |
| Device | CLASS II | Molift Mover recalled by Etac A/s | Etac | Device Malfunction | Nationwide |
| Device | CLASS II | Single Use 3-Lumen Sphincterotome V (Distal Wire guided) recalled | Olympus Corporation of the Americas | Device Malfunction | Nationwide |
| Device | CLASS II | Nasal Jejunal Feeding Tube recalled by Wilson-Cook Medical | Wilson-Cook Medical | Packaging Defects | NC |
| Device | CLASS II | Empowr Acetabular System: Liner, 10 degree Hooded, HXe+, 36H recalled | Encore Medical | Packaging Defects | 14 states |
| Device | CLASS II | Rumex Disposable Diamond Dusted ILM Elevator recalled by Vortex Surgical | Vortex Surgical | Sterility | Nationwide |
| Device | CLASS II | Naeotom Alpha.Prime recalled by Siemens Medical Solutions USA | Siemens Medical Solutions USA | Device Malfunction | Nationwide |
| Device | CLASS II | Molift 2-point sling bars (Accessory to mobile hoists) recalled | Etac | Device Malfunction | Nationwide |
| Device | CLASS II | Volk Single Use Vitrectomy Lenses Flat Vitrectomy Lens recalled | Vortex Surgical | Sterility | Nationwide |
| Device | CLASS II | Bubble Sensor for 3/8" x 3/32" tubing recalled by Maquet Cardiopulmonary | Maquet Cardiopulmonary | Device Malfunction | Nationwide |
| Device | CLASS II | LH One Step Ovulation Test Device (Urine) recalled by Changchun Wancheng | Changchun Wancheng Bio-Electron | Labeling Errors | Nationwide |
| Device | CLASS I | Axios Stent and Electrocautery-Enhanced Delivery System recalled | Boston Scientific | Other | Nationwide |
| Device | CLASS II | Single Use 3-Lumen Sphincterotome recalled by Olympus Corporation of the | Olympus Corporation of the Americas | Device Malfunction | Nationwide |
| Device | CLASS II | Disposable Triple Lumen Sphincterotome recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS I | *HOT Axios Stent and Electrocautery-Enhanced Delivery System recalled | Boston Scientific | Other | Nationwide |
| Device | CLASS II | Single Use 3-Lumen Sphincterotome recalled by Olympus Corporation of the | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS II | Single Use Sphincterotome V (Distal Wire guided) recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS II | Lumipulse G ¿-Amyloid 1-42-N Plasma Calibrators recalled | Fujirebio Diagnostics | Labeling Errors | Nationwide |
| Device | CLASS II | Vortex Disposable Forceps and Cannula recalled by Vortex Surgical | Vortex Surgical | Sterility | Nationwide |
| Device | CLASS II | CellMek SPS Sample Preparation System recalled by Beckman Coulter | Beckman Coulter | Device Malfunction | Nationwide |
| Device | CLASS II | Prismaflex Hf1000 Set recalled by Vantive Us Healthcare | Vantive US Healthcare | Packaging Defects | Nationwide |
| Device | CLASS II | Subretinal Injection Cannula VS0220.25 recalled by Vortex Surgical | Vortex Surgical | Sterility | Nationwide |
| Device | CLASS II | Vivoo Sodium Test recalled by Changchun Wancheng | Changchun Wancheng Bio-Electron | Labeling Errors | Nationwide |
| Device | CLASS II | Single Use 3-Lumen Sphincterotome V (Distal Wire guided) recalled | Olympus Corporation of the Americas | Device Malfunction | Nationwide |
| Device | CLASS II | Vivoo pH Test recalled by Changchun Wancheng | Changchun Wancheng Bio-Electron | Labeling Errors | Nationwide |
| Device | CLASS II | Disposable Triple Lumen Sphincterotome recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS II | The Girlfriend Doctor Dr. Anna Cabeca Keto-pH-Uric Acid Test Strips recalled | Changchun Wancheng Bio-Electron | Labeling Errors | Nationwide |
| Device | CLASS II | Tecfen Retractable Membrane Polisher, QTPR1267 recalled | Vortex Surgical | Sterility | Nationwide |
| Device | CLASS II | Naeotom Alpha recalled by Siemens Medical Solutions USA | Siemens Medical Solutions USA | Device Malfunction | Nationwide |
| Device | CLASS II | Perform Reversed Perip Screw 5.0mmx18mm Non Sterile recalled by Tornier | Tornier | Labeling Errors | Nationwide |
| Device | CLASS II | Lumipulse G ¿-Amyloid 1-42-N Plasma Immunoreaction Cartridges recalled | Fujirebio Diagnostics | Labeling Errors | Nationwide |
| Device | CLASS II | Single Use 3-Lumen Sphincterotome V (Distal Wire guided) recalled | Olympus Corporation of the Americas | Device Malfunction | Nationwide |
| Device | CLASS II | Single Use 3-Lumen Sphincterotome recalled by Olympus Corporation of the | Olympus Corporation of the Americas | Device Malfunction | Nationwide |
| Device | CLASS II | I.D.D. Internal Delivery Device, VS0250.25 recalled by Vortex Surgical | Vortex Surgical | Sterility | Nationwide |
| Device | CLASS II | S. Typhi/Para Typhi A Antigen recalled by Changchun Wancheng | Changchun Wancheng Bio-Electron | Labeling Errors | Nationwide |
| Device | CLASS II | MiniMed Insulin Pump recalled by Medtronic MiniMed | Medtronic MiniMed | Device Malfunction | Nationwide |
| Device | CLASS II | Oertli 1. Laser Probe OS4 Flex-Tip VK401113 2. Laser Probe recalled | Vortex Surgical | Sterility | Nationwide |
| Device | CLASS II | Lumipulse ¿-Amyloid Plasma Controls recalled by Fujirebio Diagnostics | Fujirebio Diagnostics | Labeling Errors | Nationwide |
| Device | CLASS II | Single Use 3-Lumen Sphincterotome recalled by Olympus Corporation of the | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS II | Lumipulse G pTau217/B-Amyloid 1-42 Plasma Ratio recalled | Fujirebio Diagnostics | Labeling Errors | Nationwide |
| Device | CLASS II | Olympus Single Use Electrosurgical Knife KD recalled | Olympus Corporation of the Americas | Device Malfunction | Nationwide |
| Device | CLASS II | Prismaflex St150 Set Us recalled by Vantive Us Healthcare | Vantive US Healthcare | Packaging Defects | Nationwide |
| Device | CLASS II | Single Use 3-Lumen Sphincterotome recalled by Olympus Corporation of the | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS II | Single Use 3-Lumen Sphincterotome V (Distal Wire guided) recalled | Olympus Corporation of the Americas | Device Malfunction | Nationwide |
| Device | CLASS II | Olympus Single Use Electrosurgical Knife KD recalled | Olympus Corporation of the Americas | Device Malfunction | Nationwide |
| Device | CLASS I | Axios Stent and Electrocautery-Enhanced Delivery System recalled | Boston Scientific | Other | Nationwide |
| Device | CLASS II | Somatom X.ceed recalled by Siemens Medical Solutions USA | Siemens Medical Solutions USA | Device Malfunction | Nationwide |
| Device | CLASS II | Single Use 3-Lumen Sphincterotome V (Distal Wire guided) recalled | Olympus Corporation of the Americas | Device Malfunction | Nationwide |
| Device | CLASS II | LotFancy Urinary Tract Infection Urine (UTI) Test Strips recalled | Changchun Wancheng Bio-Electron | Labeling Errors | Nationwide |
| Device | CLASS II | Empowr 3D Knee Tibial Insert 5R, VE recalled by Encore Medical | Encore Medical | Packaging Defects | 14 states |
| Device | CLASS II | Naeotom Alpha.Pro recalled by Siemens Medical Solutions USA | Siemens Medical Solutions USA | Device Malfunction | Nationwide |
| Device | CLASS II | Prismaflex Hf1000 Set recalled by Vantive Us Healthcare | Vantive US Healthcare | Packaging Defects | Nationwide |
| Device | CLASS II | Single Use 3-Lumen Sphincterotome recalled by Olympus Corporation of the | Olympus Corporation of the Americas | Device Malfunction | Nationwide |
| Device | CLASS II | Prismaflex Tpe2000 Set recalled by Vantive Us Healthcare | Vantive US Healthcare | Packaging Defects | Nationwide |
| Device | CLASS II | Backflush, VS0270.25 recalled by Vortex Surgical | Vortex Surgical | Sterility | Nationwide |
| Device | CLASS II | Single Use 3-Lumen Sphincterotome V (Distal Wire guided) recalled | Olympus Corporation of the Americas | Device Malfunction | Nationwide |
| Device | CLASS II | I2 Injection Kit, VS0500 recalled by Vortex Surgical | Vortex Surgical | Sterility | Nationwide |
| Device | CLASS II | CleverCut Single Use 3-Lumen Sphincterotome recalled | Olympus Corporation of the Americas | Device Malfunction | Nationwide |
| Device | CLASS II | Disposable Triple Lumen Sphincterotome recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS II | TID Pharos Illuminated Depressor, VS0801B recalled by Vortex Surgical | Vortex Surgical | Other | Nationwide |
| Device | CLASS II | Prismaflex M150 Set recalled by Vantive Us Healthcare | Vantive US Healthcare | Packaging Defects | Nationwide |
| Device | CLASS I | *HOT Axios Stent and Electrocautery-Enhanced Delivery System recalled | Boston Scientific | Other | Nationwide |
| Device | CLASS II | Single Use 3-Lumen Sphincterotome V (Distal Wire guided) recalled | Olympus Corporation of the Americas | Device Malfunction | Nationwide |
| Device | CLASS II | FDR Visionary Suite recalled by FUJIFILM Healthcare Americas | Fujifilm Healthcare Americas | Other | Nationwide |
| Device | CLASS II | Vivoo Protein Test recalled by Changchun Wancheng | Changchun Wancheng Bio-Electron | Labeling Errors | Nationwide |
| Device | CLASS II | 1. Laser Probe Curved recalled by Vortex Surgical | Vortex Surgical | Sterility | Nationwide |
| Device | CLASS II | Oxiris SET recalled by Vantive Us Healthcare | Vantive US Healthcare | Packaging Defects | Nationwide |
| Device | CLASS II | Single Use 3-Lumen Sphincterotome recalled by Olympus Corporation of the | Olympus Corporation of the Americas | Device Malfunction | Nationwide |
| Device | CLASS II | Prismaflex St100 Set Us recalled by Vantive Us Healthcare | Vantive US Healthcare | Packaging Defects | Nationwide |
| Device | CLASS II | Focalyx Fusion recalled by Focalyx Technologies | Focalyx Technologies | Device Malfunction | Nationwide |
| Device | CLASS II | Single Use 3-Lumen Sphincterotome V (Distal Wire guided) recalled | Olympus Corporation of the Americas | Device Malfunction | Nationwide |
| Device | CLASS II | Primsaflex M100 Set recalled by Vantive Us Healthcare | Vantive US Healthcare | Packaging Defects | Nationwide |
| Device | CLASS II | Disposable Triple Lumen Sphincterotome recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS I | Axios Stent and Electrocautery-Enhanced Delivery System recalled | Boston Scientific | Other | Nationwide |
| Device | CLASS II | Single Use 3-Lumen Sphincterotome V (Distal Wire guided) recalled | Olympus Corporation of the Americas | Device Malfunction | Nationwide |
| Device | CLASS II | Disposable Triple Lumen Sphincterotome recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS I | HOT Axios Stent and Electrocautery-Enhanced Delivery System recalled | Boston Scientific | Other | Nationwide |
| Device | CLASS II | Disposable Triple Lumen Sphincterotome recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS II | Lumipulse G pTau 217 Plasma Calibrators recalled | Fujirebio Diagnostics | Labeling Errors | Nationwide |
| Device | CLASS II | Molift Mover recalled by Etac A/s | Etac | Device Malfunction | Nationwide |
| Device | CLASS II | Single Use 3-Lumen Sphincterotome recalled by Olympus Corporation of the | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS II | Disposable Triple Lumen Sphincterotome recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS II | Exploro Highly Sensitive Male Fertility / Sperm Concentration Test recalled | Changchun Wancheng Bio-Electron | Labeling Errors | Nationwide |
| Device | CLASS II | Vitek-negative Susceptibility Cards Containing o Polymyxin recalled | Biomerieux | Sterility | Nationwide |
| Device | CLASS II | Male Fertility Sperm Test for Home Use (Cassette) recalled | Changchun Wancheng Bio-Electron | Labeling Errors | Nationwide |
| Device | CLASS II | Single Use 3-Lumen Sphincterotome recalled by Olympus Corporation of the | Olympus Corporation of the Americas | Device Malfunction | Nationwide |
| Device | CLASS II | Single Use 3-Lumen Sphincterotome recalled by Olympus Corporation of the | Olympus Corporation of the Americas | Device Malfunction | Nationwide |
| Device | CLASS II | Molift 4-point sling bars (Accessory to mobile hoists) recalled | Etac | Device Malfunction | Nationwide |
| Device | CLASS II | Lumipulse pTau 217 Plasma Controls recalled by Fujirebio Diagnostics | Fujirebio Diagnostics | Labeling Errors | Nationwide |
| Device | CLASS II | Disposable Triple Lumen Sphincterotome recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS II | Single Use 3-Lumen Sphincterotome recalled by Olympus Corporation of the | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS II | Coulter DxH Diluent recalled by Beckman Coulter | Beckman Coulter | Other | Nationwide |
| Device | CLASS II | Convenience Kits recalled by Vortex Surgical | Vortex Surgical | Sterility | Nationwide |
| Drug | CLASS I | Rheumacare capsules, Mfg in India by: Virgo UAP Pharma Pvt recalled | Handelnine Global | Lead & Heavy Metals | NY |
| Drug | CLASS II | Diclofenac Sodium, Topical Gel, 3% tube recalledDiclofenac Sodium | SUN Pharmaceutical Industries | Potency & Assay | Nationwide |
| Drug | CLASS II | Trazodone Hydrochloride, USP, 50 mg recalled by Granules PharmaceuticalsTrazodone Hydrochloride | Granules Pharmaceuticals | Other | Nationwide |
| Drug | CLASS I | Green Lumber Natural Fuel For Men capsule recalled | Green Lumber Holdings | Hidden Drug Ingredients | Nationwide |
| Drug | CLASS II | Bisoprolol Fumarate and Hydrochlorothiazide tablets recalledBisoprolol Fumarate And Hydrochlorothiazide | Unichem Pharmaceuticals USA | Nitrosamine Impurity | Nationwide |
| Food | CLASS I | Ground Beef Products recalled by CS Beef Packers | CS Beef Packers | E. coli | |
| Food | CLASS I | Juice from the Raw, Detox Greens recalled by Everpress Juice | Everpress Juice | Other | 24 states |
| Food | CLASS I | Juice from the Raw, sweet greens recalled by Everpress Juice | Everpress Juice | Other | 24 states |
| Food | CLASS III | BarbaCuban 455 Everything Sauce (Hot) recalledBarbaCuban | Prima Foods International | Undeclared Allergens | FL |
| Food | CLASS II | Deli Margherita Pizza Thin Crust recalled by WinCo FoodsWinCo | WinCo Foods | Foreign Material | 10 states |
| Food | CLASS II | spicely Organic celery salt NO Artificial Coloring NO recalled | Organic Spices | Labeling Errors | 13 states |
| Food | CLASS II | Sea Moss Gel Superfood;; sold individually recalled by Diva FamSea Moss | Diva Fam | Botulism | Nationwide |
| Food | CLASS II | Sea Moss Gel Superfood;; sold individually recalled by Diva FamSea Moss | Diva Fam | Botulism | Nationwide |
| Food | CLASS II | Cinnamon Powder recalled by Venzu TradersCinnamon | Venzu Traders | Foreign Material | CA, NV, WA |
| Food | CLASS II | Sea Moss Gel Superfood;; sold individually recalled by Diva FamSea Moss | Diva Fam | Botulism | Nationwide |
| Food | CLASS I | Juice from the Raw, upbeat recalled by Everpress Juice | Everpress Juice | Other | 24 states |
| Food | CLASS II | spicely Organic sumac NO Artificial Coloring NO Gluten recalled | Organic Spices | Labeling Errors | 13 states |
| Food | CLASS II | Gluten Free 14" Seasoned Vegan Pizza Crust recalled by Rich Products | Rich Products | Undeclared Milk | 6 states |
| Food | CLASS III | Lost and Found Energy, Sour Gummy Bear, 12pck Cans Case recalledLost | Fazt & Loud | Packaging Defects | Nationwide |
| Food | CLASS II | spicely Organic garlic salt NO Artificial Coloring NO recalled | Organic Spices | Labeling Errors | 13 states |
| Food | CLASS II | Sea Moss Gel Superfood;; sold individually recalled by Diva FamSea Moss | Diva Fam | Botulism | Nationwide |
| Food | CLASS III | BarbaCuban 90 Miles to Mojo Marinade recalledBarbaCuban | Prima Foods International | Undeclared Allergens | FL |
| Food | CLASS III | Health OptiWize Collagen Plus recalledHealth OptiWize | Optiwize | Other | Nationwide |
| Food | CLASS II | Repackaged M&Ms Peanut candies recalled by Beacon PromotionsRepackaged M&Ms | Beacon Promotions | Undeclared Allergens | 20 states |
| Food | CLASS I | Bread and Roll Mix recalled by B.C. Williams Bakery Service | B.C. Williams Bakery Service | Undeclared Milk | Nationwide |
| Food | CLASS I | Spice Cake Mix recalled by B.C. Williams Bakery Service | B.C. Williams Bakery Service | Undeclared Milk | Nationwide |
| Food | CLASS II | Sea Moss Gel Superfood;; sold individually recalled by Diva FamSea Moss | Diva Fam | Botulism | Nationwide |
| Food | CLASS III | BarbaCuban Ram Air Red Zesty Ketchup recalledBarbaCuban Ram | Prima Foods International | Undeclared Allergens | FL |
| Food | CLASS III | BarbaCuban Cubama White Truffle Sauce recalledBarbaCuban Cubama | Prima Foods International | Undeclared Allergens | FL |
| Food | CLASS I | Organic Chia Seed Black Origin: Paraguay recalled by Tradin Organics USA | Tradin Organics USA | Salmonella | CA, CO, NY |
| Food | CLASS II | Sea Moss Gel Superfood;; sold individually recalled by Diva FamSea Moss | Diva Fam | Botulism | Nationwide |
| Food | CLASS I | Juice from the Raw, spicy lemonade recalled by Everpress Juice | Everpress Juice | Other | 24 states |
| Food | CLASS III | BarbaCuban Havana Gold recalled by Prima Foods InternationalBarbaCuban Havana | Prima Foods International | Undeclared Allergens | FL |
| Food | CLASS II | Sea Moss Gel Superfood;; sold individually recalled by Diva FamSea Moss | Diva Fam | Botulism | Nationwide |
| Food | CLASS I | Juice from the Raw, pineapple mint recalled by Everpress Juice | Everpress Juice | Other | 24 states |
| Food | CLASS I | Swiss Chocolate Cake Mix recalled by B.C. Williams Bakery ServiceSwiss | B.C. Williams Bakery Service | Undeclared Milk | Nationwide |
| Food | CLASS III | Almond Despair recalled by Willy Pete's Chocolate CompanyPete's Chocolates | Willy Pete's Chocolate Company | Undeclared Tree Nuts | CT, MA, SC |
| Food | CLASS III | BarbaCuban 455 Everything Sauce (Original) recalledBarbaCuban | Prima Foods International | Undeclared Allergens | FL |
| Food | CLASS I | Juice from the Raw, cashew coffee milk recalled by Everpress Juice | Everpress Juice | Other | 24 states |
| Food | CLASS II | Sea Moss Gel Superfood;; sold individually recalled by Diva FamSea Moss | Diva Fam | Botulism | Nationwide |
| Food | CLASS II | Sea Moss Gel Superfood;; sold individually recalled by Diva FamSea Moss | Diva Fam | Botulism | Nationwide |
| Food | CLASS I | Juice from the Raw, cashew milk recalled by Everpress Juice | Everpress Juice | Other | 24 states |
| Food | CLASS II | Product is Frozen Half Shell Oysters in 15- blocks recalledProduct | Khee Trading | Norovirus | 7 states |
| Food | CLASS II | Sea Moss Gel Superfood;; sold individually recalled by Diva FamSea Moss | Diva Fam | Botulism | Nationwide |
| Food | CLASS II | Imu-Tek Immuno-5 Colostrum Powder recalled by Imu-Tek Animal HealthImu-Tek Immuno-5 | Imu-Tek Animal Health, Incorporated | Undeclared Milk | 15 states |
| Food | CLASS II | Sea Moss Gel Superfood;; sold individually recalled by Diva FamSea Moss | Diva Fam | Botulism | Nationwide |
| Food | CLASS I | Bread Crumbs, Outside The Breadbox recalled by Vh Foods | Vh Foods | Undeclared Allergens | 8 states |
| Food | CLASS II | Sea Moss Gel Superfood;; sold individually recalled by Diva FamSea Moss | Diva Fam | Botulism | Nationwide |
| Food | CLASS II | Sea Moss Gel Superfood;; sold individually recalled by Diva FamSea Moss | Diva Fam | Botulism | Nationwide |
| Food | CLASS I | Sofit, Seedless Red Dates package, 50 packages recalledSofit | Tai Phat Wholesalers | Undeclared Sulfites | 4 states |
| Food | CLASS II | Repackaged M&Ms candies recalled by Beacon PromotionsRepackaged M&Ms | Beacon Promotions | Undeclared Allergens | 20 states |
| Food | CLASS II | Sea Moss Gel Superfood;; sold individually recalled by Diva FamSea Moss | Diva Fam | Botulism | Nationwide |
| Device | CLASS II | BD Alaris" Pump Module recalled by CareFusion 303 | CareFusion 303 | Device Malfunction | Nationwide |
| Device | CLASS II | Medline medical procedure convenience kits labeled as recalled | Medline Industries | Device Malfunction | Nationwide |
| Device | CLASS II | Medical Linear Accelerator Elekta Synergy, Elekta Harmony recalled | Elekta | Device Malfunction | GA |
| Device | CLASS II | Conductivity Standard Solution recalled by NIPRO Technical Services | Nipro Technical Services | Device Malfunction | Nationwide |
| Device | CLASS II | Alphenix Infx-8000C, interventional fluoroscopic x-ray system recalled | Canon Medical System USA | Device Malfunction | Nationwide |
| Device | CLASS II | Medline medical procedure convenience kits labeled as recalled | Medline Industries | Device Malfunction | Nationwide |
| Device | CLASS II | Bandages and first aid kits: First Aid Kit 24/42PC recalled | Gold Star Distribution | Foreign Material | Nationwide |
| Device | CLASS II | Medline medical procedure convenience kits labeled as recalled | Medline Industries | Device Malfunction | Nationwide |
| Device | CLASS I | Broselow Pediatric Emergency Rainbow Tape recalled by SunMed Holdings | SunMed Holdings | Device Malfunction | Nationwide |
| Device | CLASS II | Ingenia 1.5T recalled by Philips North America | Philips North America | Other | Nationwide |
| Device | CLASS II | Medline medical procedure convenience kits labeled as recalled | Medline Industries | Device Malfunction | Nationwide |
| Device | CLASS II | Genesis Screw-In Anchor recalled by Aju Pharm Co | Aju Pharm | Packaging Defects | Nationwide |
| Device | CLASS II | Alphenix Infx-8000V, interventional fluoroscopic x-ray system recalled | Canon Medical System USA | Device Malfunction | Nationwide |
| Device | CLASS II | Pregnancy Test recalled by Gold Star Distribution | Gold Star Distribution | Foreign Material | Nationwide |
| Device | CLASS II | Interventional Fluoroscopic X-Ray System: Luminos Q.namix recalled | Siemens Medical Solutions USA | Device Malfunction | Nationwide |
| Device | CLASS II | Alphenix Infx-8000H, interventional fluoroscopic x-ray system recalled | Canon Medical System USA | Device Malfunction | Nationwide |
| Device | CLASS I | Broselow" Filled Broselow Organizer recalled by SunMed Holdings | SunMed Holdings | Device Malfunction | Nationwide |
| Device | CLASS II | Brand Name: LimFlow Vector Product Name recalled | LimFlow | Other | Nationwide |
| Device | CLASS II | Condoms, labeled as: Trojan Magnum Condoms 6/Dsp Black recalled | Gold Star Distribution | Foreign Material | Nationwide |
| Device | CLASS II | Genesis Dual Thread Screw-In Anchor recalled by Aju Pharm Co | Aju Pharm | Packaging Defects | Nationwide |
| Device | CLASS I | Broselow Domestic Complete ALS Organizer recalled by SunMed Holdings | SunMed Holdings | Device Malfunction | Nationwide |
| Device | CLASS II | AlternatiV+ Max Knotless Anchor recalled by Aju Pharm Co | Aju Pharm | Packaging Defects | Nationwide |
| Device | CLASS II | Upgrade to MR recalled by Philips North America | Philips North America | Other | Nationwide |
| Device | CLASS II | Medline medical procedure convenience kits labeled as recalled | Medline Industries | Device Malfunction | Nationwide |
| Device | CLASS II | Ingenia Elition recalled by Philips North America | Philips North America | Other | Nationwide |
| Device | CLASS II | Medline medical procedure convenience kits labeled as recalled | Medline Industries | Device Malfunction | Nationwide |
| Device | CLASS II | Medline medical procedure convenience kits labeled as recalled | Medline Industries | Device Malfunction | Nationwide |
| Device | CLASS II | Ingenia Ambition recalled by Philips North America | Philips North America | Other | Nationwide |
| Device | CLASS II | SmartPath to dStream for XR and 3.0T recalled by Philips North America | Philips North America | Other | Nationwide |
| Device | CLASS II | Zimmer Tourniquet Systems A.T.S.¿ 5000TS Tourniquet Systems recalled | Zimmer Surgical | Device Malfunction | OH |
| Device | CLASS II | Alphenix Infx-8000F, interventional fluoroscopic x-ray system recalled | Canon Medical System USA | Device Malfunction | Nationwide |
| Device | CLASS II | Medline medical procedure convenience kits labeled as recalled | Medline Industries | Device Malfunction | Nationwide |
| Device | CLASS II | Evolution Upgrade 3.0T recalled by Philips North America | Philips North America | Other | Nationwide |
| Device | CLASS II | Toothbrushes, labeled as: Oral B Tooth Brush Shiny Clean Soft recalled | Gold Star Distribution | Foreign Material | Nationwide |
| Device | CLASS II | PearMatrix P-15 Peptide Enhanced Bone Graft Bone Graft, 1.0cc recalled | Cerapedics | Other | Nationwide |
| Device | CLASS II | Ingenia Elition recalled by Philips North America | Philips North America | Other | Nationwide |
| Device | CLASS II | Feminine hygiene products, labeled as recalled by Gold Star Distribution | Gold Star Distribution | Foreign Material | Nationwide |
| Device | CLASS II | Genesis Knotless Anchor recalled by Aju Pharm Co | Aju Pharm | Packaging Defects | Nationwide |
| Device | CLASS II | Chest Drainage Units and Accessories recalled by Cardinal Health 200 | Cardinal Health 200 | Device Malfunction | Nationwide |
| Device | CLASS II | Ingenia 3.0T CX recalled by Philips North America | Philips North America | Other | Nationwide |
| Device | CLASS II | MR 7700. Product Code (REF): (1) 782120, (2) 782153. MR systems recalled | Philips North America | Other | Nationwide |
| Device | CLASS II | Ingenia 3.0T recalled by Philips North America | Philips North America | Other | Nationwide |
| Device | CLASS II | Zimmer Tourniquet Systems A.T.S.¿ 3200TS Tourniquet Systems recalled | Zimmer Surgical | Device Malfunction | OH |
| Device | CLASS II | Medline medical procedure convenience kits labeled as recalled | Medline Industries | Device Malfunction | Nationwide |
| Device | CLASS II | Medline medical procedure convenience kits labeled as recalled | Medline Industries | Device Malfunction | Nationwide |
| Device | CLASS II | Medline medical procedure convenience kits labeled as recalled | Medline Industries | Device Malfunction | Nationwide |
| Device | CLASS II | Fixone Hybrid Anchor recalled by Aju Pharm Co | Aju Pharm | Packaging Defects | Nationwide |
| Device | CLASS II | Fixone Biocomposite Anchor recalled by Aju Pharm Co | Aju Pharm | Packaging Defects | Nationwide |
| Device | CLASS II | BEAR Implant recalled by Miach Orthopaedics | Miach Orthopaedics | Other | Nationwide |
| Device | CLASS II | Evolution Upgrade 1.5T recalled by Philips North America | Philips North America | Other | Nationwide |
| Device | CLASS II | Medline medical procedure convenience kits labeled as recalled | Medline Industries | Device Malfunction | Nationwide |
| Device | CLASS II | Medline medical procedure convenience kits labeled as recalled | Medline Industries | Device Malfunction | Nationwide |
| Device | CLASS I | Broselow Pediatric Emergency Rainbow Tape recalled by SunMed Holdings | SunMed Holdings | Device Malfunction | Nationwide |
| Device | CLASS II | Interventional Fluoroscopic X-Ray System: Luminos Q.namix recalled | Siemens Medical Solutions USA | Device Malfunction | Nationwide |
| Device | CLASS II | Ingenia Ambition recalled by Philips North America | Philips North America | Other | Nationwide |
| Device | CLASS II | Genesis Push-In Suture Anchor recalled by Aju Pharm Co | Aju Pharm | Packaging Defects | Nationwide |
| Device | CLASS II | SmartPath to dStream for 3.0T recalled by Philips North America | Philips North America | Other | Nationwide |
| Device | CLASS II | Medline medical procedure convenience kits labeled as recalled | Medline Industries | Device Malfunction | Nationwide |
| Device | CLASS II | AlternatiV+ Screw-In Anchor recalled by Aju Pharm Co | Aju Pharm | Packaging Defects | Nationwide |
| Device | CLASS II | Medline medical procedure convenience kits labeled as recalled | Medline Industries | Device Malfunction | Nationwide |
| Device | CLASS II | Central Line Dressing Kit recalled by LSL Healthcare | LSL Healthcare | Packaging Defects | Nationwide |
| Drug | CLASS II | INON ACE Antacid tablets (magnesium aluminosilicate recalledInon Ace | Sato Pharmaceutical | Other | CA, HI |
| Drug | CLASS II | methylprednisolone tablets, USP Dosepak, 4 mg recalled by GreenstoneMethylprednisolone | Greenstone | Other | Nationwide |
| Drug | CLASS III | Glycopyrrolate Oral Solution, 1 mg recalled by Novadoz PharmaceuticalsGlycopyrrolate | Novadoz Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS II | Sterile Water for Irrigation, Single-Dose recalled by Baxter HealthcareSterile Water | Baxter Healthcare | Particulate Matter | Nationwide |
| Drug | CLASS III | parodontax (cetylpyridinium chloride)Active Gum Health recalledParodontax | Haleon US Holdings | Other | Nationwide |
| Food | CLASS II | Roasted Pumpkin & White Cheddar Tamales Ingredients recalled | Prima Vera Nueva | Listeria | CA, NV |
| Food | CLASS II | Goldenroot Lemon Ginger Hibiscus Ginger Beer recalled by Weaver's BrewGoldenroot | Weaver's Brew | Processing Deviation | CA, TX |
| Food | CLASS II | Hannaford hamburger dill pickle chips (1 PT) recalledHannaford | Mount Olive Pickle Company | Foreign Material | ME, NY |
| Food | CLASS II | Qunol, Extra Strength Turmeric Capsule recalledQunol | Quten Research Institiute | Mold | 30 states |
| Food | CLASS II | Mushroom, Spinach & Salsa Tamales No Dairy Ingredients recalled | Prima Vera Nueva | Listeria | CA, NV |
| Food | CLASS II | BBQ Chipotle Bean & White Cheddar Tamales Ingredients recalledBBQ Chipotle | Prima Vera Nueva | Listeria | CA, NV |
| Food | CLASS III | Preserved Mustard in Soybean Oil recalled by New Way ImportPreserved Mustard | New Way Import | Undeclared Allergens | CA |
| Food | CLASS II | Goldenroot Lemon Ginger Elderberry Ginger Beer recalled by Weaver's BrewGoldenroot | Weaver's Brew | Processing Deviation | CA, TX |
| Food | CLASS II | Higher Harvest by H-e-b Dairy Free Coconut Based Yogurt recalledHigher Harvest | Plant Based Innovations | Undeclared Tree Nuts | TX |
| Food | CLASS I | a.) Live it Up brand Super Greens recalled by Superfoodsit Up | Superfoods | Salmonella | Nationwide |
| Food | CLASS II | Goldenroot Lemon Double Ginger, Ginger Beer recalled by Weaver's BrewGoldenroot | Weaver's Brew | Processing Deviation | CA, TX |
| Food | CLASS II | Goldenroot Yuzu Ginger Lemongrass Ginger Beer recalled by Weaver's BrewGoldenroot Yuzu | Weaver's Brew | Processing Deviation | CA, TX |
| Food | CLASS I | Live it Up Super Greens recalled by Superfoodsit Up | Superfoods | Salmonella | Nationwide |
| Food | CLASS II | Roasted Green Chile Tamales NO Dairy Ingredients recalled | Prima Vera Nueva | Listeria | CA, NV |
| Food | CLASS II | McCafe Premium Roast Decaf Coffee K-Cup Pods recalledMcCafe | Keurig DR Pepper | Packaging Defects | CA, IN, NV |
| Food | CLASS II | Black Bean Bonanza Tamales with Black Beans NO Dairy recalled | Prima Vera Nueva | Listeria | CA, NV |
| Food | CLASS II | Black Bean Bonanza Tamales with Black Beans recalled by Prima Vera Nueva | Prima Vera Nueva | Listeria | CA, NV |
| Food | CLASS II | Butternut Squash Tamales With Roasted Green Chiles recalledButternut Squash | Prima Vera Nueva | Listeria | CA, NV |
| Food | CLASS II | Butternut Squash Tamales with Roasted Green Chiles recalledButternut Squash | Prima Vera Nueva | Listeria | CA, NV |
| Food | CLASS II | Goldenroot Lemon Ginger Jalapeno Ginger Beer recalled by Weaver's BrewGoldenroot | Weaver's Brew | Processing Deviation | CA, TX |
| Food | CLASS II | Roasted Green Chile & Jack Cheese Tamales Ingredients recalled | Prima Vera Nueva | Listeria | CA, NV |
| Food | CLASS II | Mushroom, Spinach & Salsa Tamales recalled by Prima Vera Nueva | Prima Vera Nueva | Listeria | CA, NV |
| Food | CLASS II | Soma Kitchen Natural Asafoetida recalled by Bharat BazarSoma | Bharat Bazar | Undeclared Wheat & Gluten | CA |
| Food | CLASS I | Frozen, Raw Pork Boneless Loins recalled by Mays Chemical Company of | Mays Chemical Company of Puerto Rico | Foreign Material | |