Latest FDA Food & Drug Recalls
Drug and food enforcement actions from FDA, including recalls, market withdrawals, and safety alerts.
FDA Recalls
Olympus Recalls ShockPulse-SE Lithotripsy System Probes Due to Recognition Issues
FDA · 3d ago
FDA Recalls
Advanced Bionics Recalls Sky CI M90 Sound Processors Due to Labeling Error
FDA · 3d ago
FDA Recalls
Olympus Recalls ShockPulse-SE Lithotripsy Systems Due to Mis-wired Components
FDA · 3d ago
FDA Recalls
Vascutek, Ltd. Recalls Gelsoft Plus and Gelweave Vascular Devices Due to Incorrect Shelf Life Labeling
FDA · 3d ago
FDA Recalls
Diagnostica Stago Recalls STA Liatest Free Protein S Kits for Inaccurate Test Results
FDA · 4d ago
FDA Recalls
Olympus Recalls ShockPulse-SE Lithotripsy System Reusable Probes Due to Recognition Issues
FDA · 4d ago
FDA Recalls
Datascope Corp. Recalls CS100 IABP Devices Due to Battery Specification Updates
FDA · 4d ago
FDA Recalls
Siemens Healthcare Diagnostics Recalls Atellica CH Urine Albumin Test Kits Due to Inaccurate Results
FDA · 4d ago
FDA Recalls
Datascope Corp. Recalls CS300 IABP Devices to Update Battery Specifications
FDA · 4d ago
FDA Recalls high
GE Healthcare Recalls Centricity Universal Viewer Zero Footprint Client Due to Patient Data Mismatch
FDA · 4d ago
FDA Recalls high
Roche Diagnostics Recalls cobas pro Integrated Solutions Due to Software Defect
FDA · 4d ago
FDA Recalls
ESAOTE S.P.A. Recalls Endocavity Ultrasonic Probes Due to Potential Liquid Leakage
FDA · 4d ago
FDA Recalls
Aesculap Inc. Recalls MINOP Trocar Devices Due to Incorrect Shaft Length
FDA · 4d ago
FDA Recalls high
Staar Surgical AG Recalls EVO+ Visian Toric Implantable Collamer Lenses Due to Labeling Error
FDA · 4d ago
FDA Recalls high
Abiomed Recalls Impella RP Heart Pumps Over Sensor Malfunction Risks
FDA · 4d ago
FDA Recalls
Olympus Recalls ShockPulse-SE Lithotripsy System Generators Over Recognition Failure
FDA · 4d ago
FDA Recalls high
Abiomed, Inc. Issues Recall for Impella RP with SmartAssist Over Sensor Malfunction
FDA · 4d ago
FDA Recalls
Olympus Recalls Single Use Biopsy Valves Due to Rubber Fragment Detachment Risk
FDA · 4d ago
FDA Recalls high
Abiomed Recalls Impella RP Flex with SmartAssist Heart Pumps Due to Sensor Malfunction
FDA · 4d ago
FDA Recalls high
Olympus Recalls Single Use Biopsy Valves Due to Potential Rubber Fragment Detachment
FDA · 4d ago
FDA Recalls
Bader Enterprises, Inc. Recalls Premium Food Bubble Gum Over Undeclared Colors
FDA · 4d ago
FDA Recalls
Bader Enterprises Recalls Premium Food Jordan Almonds Over Undeclared Wheat and Colors
FDA · 4d ago
FDA Recalls
Italianway Import, Inc. Recalls Vergani 1944 Milano Gluten-Free Pandoro Due to Potential Teflon Contamination
FDA · 4d ago
FDA Recalls high
Juniper Granola, LLC Recalls Junebar Snack Bars Due to Undeclared Milk and Soy
FDA · 4d ago
FDA Recalls
Tippy Toes Apple Pear Banana Baby Food Recalled Over Patulin Contamination Concerns
FDA · 4d ago
FDA Recalls high
Juniper Granola Recalls Junebar Chocolate Cherry Snack Bars Due to Undeclared Milk and Soy
FDA · 4d ago
FDA Recalls high
SILINTAN 25/pills Recalled Nationwide Due to Undeclared Meloxicam
FDA · 4d ago
FDA Recalls
Acme United Corporation Recalls Children's Healthcare of Atlanta Hand Sanitizing Wipes
FDA · 4d ago
FDA Recalls
Acme United Corporation Recalls BZK Antiseptic Towelettes Due to Manufacturing Deviations
FDA · 4d ago
FDA Recalls
ACME UNITED CORPORATION Recalls WP WipesPlus Hand Sanitizing Wipes Due to Manufacturing Deviations
FDA · 4d ago
FDA Recalls
Acme United Corporation Recalls Green Guard Antiseptic Wipes Due to Manufacturing Deviations
FDA · 4d ago
FDA Recalls
Radnostix Recalls Sodium Iodide I-131 Therapeutic Oral Solution Due to Particulate Matter
FDA · 4d ago
FDA Recalls
Cipla USA Inc. Issues Nationwide Recall for Nilotinib Capsules Due to Appearance Defects
FDA · 4d ago
FDA Recalls
Harbin Jixianglong Biotech Co. Issues Nationwide Recall of Semaglutide Over Manufacturing Deviations
FDA · 4d ago
FDA Recalls
Acme United Corporation Recalls Dukal BZK Antiseptic Towelettes Due to CGMP Deviations
FDA · 4d ago
FDA Recalls
Medi-First Antiseptic Wipes Recalled Nationwide Due to Manufacturing Deviations
FDA · 4d ago
FDA Recalls
ACME UNITED CORPORATION Recalls Max Packaging Antibacterial Towelettes Due to CGMP Deviations
FDA · 4d ago
FDA Recalls
ACME UNITED CORPORATION Recalls Antimicrobial Alcohol Hand Wipes Due to CGMP Deviations
FDA · 4d ago
FDA Recalls
Teva Pharmaceuticals Recalls Metoprolol Succinate Extended-Release Tablets Due to Dissolution Failure
FDA · 4d ago
FDA Recalls
ACME UNITED CORPORATION Recalls Dynarex Obstetrical Towelettes Cleanser Due to CGMP Deviations
FDA · 4d ago
FDA Recalls
HTO Nevada Inc. Issues Recall for Maximum Zone 1 Lidocaine Cream Due to Stability Concerns
FDA · 4d ago
FDA Recalls
Acme United Corporation Recalls First Aid Only Hand Sanitizing Wipes Due to Manufacturing Deviations
FDA · 4d ago
FDA Recalls
Acme United Corporation Recalls Med-Nap BZK Antiseptic Towelettes Due to CGMP Deviations
FDA · 4d ago
FDA Recalls
ACME United Corporation Recalls Savannah Antibacterial Towelettes Due to CGMP Deviations
FDA · 4d ago
FDA Recalls
Acme United Corporation Recalls Med-Nap Cleansing Towelettes Due to CGMP Deviations
FDA · 4d ago
FDA Recalls
HTO Nevada Inc. Recalls Zone 2 Lidocaine Cream Over Stability Concerns
FDA · 4d ago
FDA Recalls
HTO Nevada Inc. Issues Nationwide Recall of VASOCAINE Spray Due to Stability Concerns
FDA · 4d ago
FDA Recalls
ACME UNITED CORPORATION Recalls Wipes Plus Hand Sanitizing BZK Wipes Due to CGMP Deviations
FDA · 4d ago
FDA Recalls
Acme United Corporation Recalls First Aid Only BZK Antiseptic Towelettes Due to CGMP Deviations
FDA · 4d ago
FDA Recalls high
Harbin Jixianglong Biotech Recalls Semaglutide for Compounding Due to CGMP Deviations
FDA · 4d ago
FDA Recalls
Major Pharmaceuticals Recalls Midodrine Hydrochloride Tablets Over Packaging Defect
FDA · 4d ago
FDA Recalls
Acme United Corporation Recalls Dynarex BZK Antiseptic Towelettes Due to Manufacturing Deviations
FDA · 4d ago
FDA Recalls
Acme United Corporation Recalls Med Nap Benzalkonium Chloride Antiseptic Towelettes Due to CGMP Deviations
FDA · 4d ago
FDA Recalls
Cipla USA Inc. Issues Voluntary Recall for Nilotinib Capsules Due to Stability Test Failure
FDA · 4d ago
FDA Recalls
Agiliti Health Recalls Adapt Pump Support Surfaces Due to Software Malfunction
FDA · Mar 11, 2026
FDA Recalls
Medline Industries Recalls Nail Kits Due to Potential Sterility Concerns
FDA · Mar 11, 2026
FDA Recalls
Edermy LLC Issues Recall for PIE Trolley System Model 2005 Due to Lack of FDA Clearance
FDA · Mar 11, 2026
FDA Recalls high
Olympus Recalls Inner Sheaths Due to Risk of Ceramic Tip Breakage
FDA · Mar 11, 2026
FDA Recalls
Hitachi Recalls PROBEAT-CR Proton Beam Therapy System Due to Software Anomaly
FDA · Mar 11, 2026
FDA Recalls high
Medline Industries Recalls Medical Kits Containing Tego Connectors Due to Seal Defects
FDA · Mar 11, 2026
FDA Recalls high
Olympus Recalls Inner Sheath Model A2642 Over Reports of Breaking Ceramic Tips
FDA · Mar 11, 2026
FDA Recalls high
Medline Industries Recalls Over 10,000 Convenience Kits Due to Sterility Concerns
FDA · Mar 11, 2026
FDA Recalls
Medline Recalls Over 3.5 Million Units of Sterile Saline Wound Wash Due to Sterility Concerns
FDA · Mar 11, 2026
FDA Recalls
Encore Medical Recalls EMPOWR 3D KNEE Implants Due to Incorrect Labeling
FDA · Mar 11, 2026
FDA Recalls
Olympus Corporation Recalls Cystoscope Outer Sheaths Due to Laser Incompatibility
FDA · Mar 11, 2026
FDA Recalls
Olympus Recalls Resection Sheaths Over Ceramic Tip Breakage Risk
FDA · Mar 11, 2026
FDA Recalls
Remel, Inc. Issues Recall for Campy CVA Medium Over Bacterial Recovery Concerns
FDA · Mar 11, 2026
FDA Recalls
Olympus Recalls Inner Sheath 21 Fr. Model A2660T Over Ceramic Tip Breakage Concerns
FDA · Mar 10, 2026
FDA Recalls
Olympus Issues Recall for Resection Sheaths Due to Risk of Ceramic Tip Breakage
FDA · Mar 10, 2026
FDA Recalls
Edermy LLC Recalls PIE PAK Medical Devices Due to Lack of 510K Clearance
FDA · Mar 10, 2026
FDA Recalls
Olympus Recalls Resection Inner Sheaths Due to Ceramic Tip Breakage
FDA · Mar 10, 2026
FDA Recalls
Medline Industries Recalls Meijer Sterile Saline Wound Wash Over Sterility Concerns
FDA · Mar 10, 2026
FDA Recalls high
Olympus Recalls Inner Sheaths Used in Gynecological Procedures Due to Breaking Ceramic Tips
FDA · Mar 10, 2026
FDA Recalls
Olympus Issues Recall for Resection Sheath Due to Risk of Ceramic Tip Breakage
FDA · Mar 10, 2026
FDA Recalls
Encore Medical, LP Recalls Reverse Shoulder Prosthesis (RSP) Humeral Socket Inserts Due to Labeling Error
FDA · Mar 10, 2026
FDA Recalls
Olympus Recalls Resection Sheaths Over Risk of Ceramic Tip Breakage
FDA · Mar 10, 2026
FDA Recalls high
Medline Industries Recalls IR Packs and Dialysis Insertion Kits Due to Faulty Tego Connectors
FDA · Mar 10, 2026
FDA Recalls
Medline Industries Recalls Nail Kits Due to Potential Sterility Issues in Wound Wash
FDA · Mar 10, 2026
FDA Recalls
Medtronic Recalls Octopus Nuvo Tissue Stabilizers Due to Assembly Error
FDA · Mar 10, 2026
FDA Recalls
Olympus Corporation Recalls Resection Inner Sheaths Due to Ceramic Tip Breakage Risk
FDA · Mar 10, 2026
FDA Recalls
Olympus Corporation of the Americas Recalls Inner Sheath Devices Due to Breaking Ceramic Tips
FDA · Mar 10, 2026
FDA Recalls
Olympus Recalls Resection Sheaths Due to Risk of Ceramic Tip Breakage
FDA · Mar 10, 2026
FDA Recalls high
Olympus Issues Recall for Inner Sheath Used in Urological Procedures Due to Breaking Ceramic Tips
FDA · Mar 10, 2026
FDA Recalls
Olympus Corporation Recalls Resection Sheaths Due to Risk of Ceramic Tip Breakage
FDA · Mar 10, 2026
FDA Recalls high
Medline Industries Recalls Over 14,000 Dialysis Kits and Trays Due to Tego Connector Seal Defects
FDA · Mar 10, 2026
FDA Recalls
Olympus Recalls Inner Sheaths Used in Urological and Gynecological Procedures Due to Breakage Risk
FDA · Mar 10, 2026
FDA Recalls high
MRIMed Inc. Recalls MRI LED Mobile Exam Light Batteries Due to Overheating and Smoke Hazard
FDA · Mar 10, 2026
FDA Recalls
Olympus Corporation Recalls Resection Sheaths Due to Risk of Ceramic Tip Breaking
FDA · Mar 10, 2026
FDA Recalls
Encore Medical, LP Recalls Reverse Shoulder Prosthesis Humeral Socket Inserts Due to Incorrect Labeling
FDA · Mar 10, 2026
FDA Recalls high
Medline Industries Recalls Dialysis Dressing Change Kits Due to Tego Connector Seal Defects
FDA · Mar 10, 2026
FDA Recalls high
Medline Industries Recalls Dialysis On/Off Kits Due to Tego Connector Seal Issues
FDA · Mar 10, 2026
FDA Recalls high
Prime Food Processing LLC Recalls Dried Croaker Fish Due to Uneviscerated Fish Hazard
FDA · Mar 10, 2026
FDA Recalls
Lubna Quality Products Inc. Recalls Mung Beans in Texas and Louisiana Due to Pesticide
FDA · Mar 10, 2026
FDA Recalls
Valley Springs Artesian Gold Recalls Bottled Water Due to Insanitary Conditions
FDA · Mar 10, 2026
FDA Recalls high
Oregon Potato Company Recalls IQF Blueberries Due to Listeria monocytogenes Risk
FDA · Mar 10, 2026
FDA Recalls
SB FOOD LLC Recalls Yoyo Gummy Assorted Flavor Over Unallowed Color Additive
FDA · Mar 10, 2026
FDA Recalls
SB FOOD LLC Recalls Yoyo Gummy Tropical Flavor Over Unapproved Color Additive
FDA · Mar 10, 2026
FDA Recalls
Valley Springs Steamed Distilled Water Recall Issued Due to Insanitary Bottling Conditions
FDA · Mar 10, 2026
FDA Recalls
SB FOOD LLC Recalls Yoyo Gummy Grape Plus Flavor Over Unallowed Color Additive
FDA · Mar 10, 2026
FDA Recalls high
MIN JIANG FOOD STORE INC Recalls Frozen Fish Balls Due to Undeclared Wheat and Sesame
FDA · Mar 10, 2026
FDA Recalls high
Wellsley Farms Farm-Raised Atlantic Salmon Recalled Due to Listeria Risk
FDA · Mar 10, 2026
FDA Recalls high
Navitas Organics Recalls Organic Chia Seeds Due to Potential Salmonella Contamination
FDA · Mar 10, 2026
FDA Recalls
Tengen USA Trading Corp Recalls YO!MAN Lettuce Due to Undeclared Cyclamates
FDA · Mar 10, 2026
FDA Recalls
Tengen USA Trading Corp Recalls YO!MAN Cucumber Due to Undeclared Cyclamates
FDA · Mar 10, 2026
FDA Recalls
Valley Springs Artesian Gold Recalls Bottled Water Over Insanitary Conditions
FDA · Mar 10, 2026
FDA Recalls
Wizcure Pharmaa Recalls Fluorescein Sodium Ophthalmic Strips Over Sterility Concerns
FDA · Mar 10, 2026
FDA Recalls
Agebox Recalls iKids-Growth Capsules Due to Undeclared Ibutamoren
FDA · Mar 10, 2026
FDA Recalls high
Vista Meibo Tears Eye Drops Recalled Nationwide Due to Sterility Concerns
FDA · Mar 10, 2026
FDA Recalls high
Agebox Recalls iKids-Growth Night Formula Due to Undeclared Ibutamoren
FDA · Mar 10, 2026
FDA Recalls high
Vista Gonio Eye Lubricant Recall Issued Due to Sterility Concerns
FDA · Mar 10, 2026
FDA Recalls high
LEO Pharma Inc. Recalls Adbry Injection Due to Potential Wool Fiber Contamination
FDA · Mar 10, 2026
FDA Recalls high
Vista Gel Hypromellose Eye Drops Recalled Nationwide Due to Sterility Concerns
FDA · Mar 10, 2026
FDA Recalls
AvKARE Issues Voluntary Recall for Amantadine HCl Capsules Due to Dissolution Failure
FDA · Mar 10, 2026
FDA Recalls
Slate Run Pharmaceuticals Recalls Eptifibatide Injection Due to Labeling Error
FDA · Mar 10, 2026
FDA Recalls
Wizcure Pharmaa Recalls Vista Tears Eye Drops Nationwide Over Sterility Concerns
FDA · Mar 10, 2026
FDA Recalls high
Wizcure Pharmaa Recalls Bio Glo Fluorescein Sodium Ophthalmic Strips Due to Sterility Concerns
FDA · Mar 10, 2026
FDA Recalls high
BioGlo Fluorescein Sodium Ophthalmic Strips Recalled Due to Sterility Concerns
FDA · Mar 10, 2026
FDA Recalls
Centinel Spine Recalls Prodisc C SK Cervical Disc Replacement Devices Due to Mislabeled Sizing
FDA · Mar 4, 2026
FDA Recalls
Medline Industries Recalls 154,427 Convenience Kits Over Sterility Concerns
FDA · Mar 4, 2026
FDA Recalls high
Medline Industries Recalls Chest/Breast Convenience Kits Due to Sterility Concerns
FDA · Mar 4, 2026
FDA Recalls
Medline Industries Recalls Over 14 Million Surgical Drapes Due to Sterility Concerns
FDA · Mar 4, 2026
FDA Recalls
Medline Industries Recalls Over 117,000 Convenience Kits Due to Sterility Concerns
FDA · Mar 4, 2026
FDA Recalls
Medline Industries Recalls Urology Convenience Kits Over Sterility Assurance Concerns
FDA · Mar 4, 2026
FDA Recalls high
Medline Industries Recalls C-Section Convenience Kits Due to Sterility Assurance Concerns
FDA · Mar 4, 2026
FDA Recalls high
Medline Industries Recalls 30,958 Convenience Kits Over Sterility Concerns
FDA · Mar 4, 2026
FDA Recalls
Medline Industries Recalls Over 39,000 Convenience Kits Due to Sterility Concerns
FDA · Mar 4, 2026
FDA Recalls high
Medline Industries Recalls Basic Nerve Block Trays Due to Sterilization Calibration Issues
FDA · Mar 4, 2026
FDA Recalls
Intuitive Surgical Recalls Da Vinci 5 Surgical Consoles Due to Software Error
FDA · Mar 4, 2026
FDA Recalls
Medline Industries Recalls Arthroscopy Kits and Trays Due to Sterility Concerns
FDA · Mar 4, 2026
FDA Recalls
Medline Industries Recalls Surgical Convenience Kits Over Sterility Concerns
FDA · Mar 4, 2026
FDA Recalls high
Olympus Recalls High Flow Insufflation Units Due to Software-Related Overpressure Risk
FDA · Mar 4, 2026
FDA Recalls
Medline Industries Recalls 4,853 Convenience Kits Over Sterilization Calibration Issues
FDA · Mar 3, 2026
FDA Recalls high
Medline Industries Recalls Dental Packs Due to Potential Sterility Issues
FDA · Mar 3, 2026
FDA Recalls
Integra LifeSciences Recalls MEDIHONEY Calcium Alginate Dressings Due to Potential Sterility Breach
FDA · Mar 3, 2026
FDA Recalls
Medline Industries Recalls 5,346 Medical Convenience Kits Over Sterility Concerns
FDA · Mar 3, 2026
FDA Recalls high
Medica Corporation Recalls Capillary Tube Kits Due to Inaccurate Potassium Results
FDA · Mar 3, 2026
FDA Recalls
Medline Industries Recalls Over 193,000 Surgical Packs Due to Sterilization Concerns
FDA · Mar 3, 2026
FDA Recalls
Medline Industries Recalls Convenience Kits Over Sterility Concerns
FDA · Mar 3, 2026
FDA Recalls
Stryker Corporation Recalls MOLLI 2 System Components Over Marker Dislodgement Risk
FDA · Mar 3, 2026
FDA Recalls
Medline Industries Recalls Over 27,000 Convenience Kits Due to Sterility Concerns
FDA · Mar 3, 2026
FDA Recalls
Medline Industries Recalls Over 70 Million Surgical Gowns Due to Sterility Concerns
FDA · Mar 3, 2026
FDA Recalls high
Medline Industries Recalls 3,561 Medical Convenience Kits Over Sterility Concerns
FDA · Mar 3, 2026
FDA Recalls high
Olympus Recalls Thunderbeat Surgical Devices Due to Adverse Event Reports
FDA · Mar 3, 2026
FDA Recalls
Medline Industries Recalls 7,494 Neuro Convenience Kits Over Sterility Concerns
FDA · Mar 3, 2026
FDA Recalls high
Medline Industries Recalls Over 4,700 Convenience Kits Due to Sterility Concerns
FDA · Mar 3, 2026
FDA Recalls
Medline Recalls Convenience GI Kits Over Potential Sterility Assurance Issues
FDA · Mar 3, 2026
FDA Recalls high
Medline Industries Recalls Burn Packs Over Sterilization Equipment Calibration Issues
FDA · Mar 3, 2026
FDA Recalls high
Medline Industries Recalls Over 12,000 Surgical Convenience Kits Due to Sterility Concerns
FDA · Mar 3, 2026
FDA Recalls high
Baxter Healthcare Recalls Spectrum IQ Infusion Pumps Due to Missing Safety Testing
FDA · Mar 3, 2026
FDA Recalls
Medline Industries Recalls Convenience Kits Over Potential Sterility Assurance Issues
FDA · Mar 3, 2026
FDA Recalls
Medline Industries Recalls Convenience Kits Due to Potential Sterility Assurance Issues
FDA · Mar 3, 2026
FDA Recalls high
Medline Industries Recalls LVAD Driveline and Central Line Dressing Trays Over Sterility Concerns
FDA · Mar 3, 2026
FDA Recalls
Medline Industries Recalls PPE Kits Due to Potential Sterility Issues
FDA · Mar 3, 2026
FDA Recalls high
Olympus Recalls High Flow Insufflation Units Over Software-Related Overpressure Risk
FDA · Mar 3, 2026
FDA Recalls
Medline Industries Recalls Lithotomy Packs Due to Potential Sterility Concerns
FDA · Mar 3, 2026
FDA Recalls high
Medline Industries Recalls 9,051 Convenience Kits Over Sterility Assurance Concerns
FDA · Mar 3, 2026
FDA Recalls high
Medline Industries Recalls Tracheostomy Convenience Kits Due to Sterility Concerns
FDA · Mar 3, 2026
FDA Recalls
Medline Industries Recalls General Closure Convenience Kits Over Sterility Assurance Concerns
FDA · Mar 3, 2026
FDA Recalls high
Medline Industries Recalls 82,597 Surgical Convenience Kits Over Sterility Concerns
FDA · Mar 3, 2026
FDA Recalls high
Olympus Recalls High Flow Insufflation Units Due to Overpressure Risk
FDA · Mar 3, 2026
FDA Recalls
Integra LifeSciences Recalls Private Label CVS Wound Care Products Over Sterility Concerns
FDA · Mar 3, 2026
FDA Recalls
Medline Industries Recalls Surgical and Medical Convenience Kits Over Sterility Concerns
FDA · Mar 3, 2026
FDA Recalls
Auris Health Recalls MONARCH Bronchoscopy Platform Due to Software Malfunction
FDA · Mar 3, 2026
FDA Recalls high
Wilson-Cook Medical Inc. Recalls Teslatome Bipolar Sphincterotomes Due to Electrical Hazard
FDA · Mar 3, 2026
FDA Recalls high
Medline Industries Recalls Over 926,000 IV Administration and Extension Sets Due to Connector Failure
FDA · Mar 3, 2026
FDA Recalls high
Medline Industries Recalls Admit Kits Due to Potential Sterility Compromise
FDA · Mar 3, 2026
FDA Recalls
Medline Industries Recalls Convenience Kits Over Potential Sterility Concerns
FDA · Mar 3, 2026
FDA Recalls high
Olympus Corporation Recalls Thunderbeat Surgical Devices Due to Adverse Event Reports
FDA · Mar 3, 2026
FDA Recalls high
Medline Industries Recalls Drape Pack-Choice Convenience Kits Over Sterility Concerns
FDA · Mar 3, 2026
FDA Recalls high
Olympus Recalls Thunderbeat Surgical Devices Following Reports of Adverse Events
FDA · Mar 3, 2026
FDA Recalls
Medline Industries Recalls Convenience Kits Due to Potential Sterility Concerns
FDA · Mar 3, 2026
FDA Recalls high
Integra LifeSciences Recalls MediHoney Gel Due to Potential Sterile Barrier Breach
FDA · Mar 3, 2026
FDA Recalls
Bard Peripheral Vascular Recalls Hickman and Broviac Catheter Trays Over Sterility Risks
FDA · Mar 3, 2026
FDA Recalls high
Medline Recalls Triple Lumen Insertion Kits Over Sterilization Equipment Calibration Issues
FDA · Mar 3, 2026
FDA Recalls
Immunotech A.S. Issues Recall for Estrone RIA Kits Over Inaccurate Test Results
FDA · Mar 3, 2026
FDA Recalls
Woodland Foods LLC Recalls Woodland Gourmet Arrowroot Flour Due to Foreign Material
FDA · Mar 3, 2026
FDA Recalls high
Lotus Mom Corporation Recalls Brass Tope Over Potential Lead Contamination
FDA · Mar 3, 2026
FDA Recalls high
H & N Group Inc. Recalls Frozen Cooked Shrimp Due to Potential Cesium-137 Contamination
FDA · Mar 3, 2026
FDA Recalls high
Reser's Fine Foods Recalls Molly Kitchen's Tuna Salad Due to Undeclared Fish Allergen
FDA · Mar 3, 2026
FDA Recalls high
Pure Solutions, Inc. Recalls Sleep Supplements Due to Undeclared Milk Allergen
FDA · Mar 3, 2026
FDA Recalls high
Why Not Natural Moringa Capsules Recalled Due to Potential Salmonella Contamination
FDA · Mar 3, 2026
FDA Recalls
Philips North America Recalls Spectral CT 7500 on Rails Over Potential Rotor Part Displacement
FDA · Feb 25, 2026
FDA Recalls
Medline Industries Recalls Mercy Circumcision Trays Due to Compromised Packaging
FDA · Feb 25, 2026
FDA Recalls high
Medline Industries Recalls Reprocessed ViewFlex Xtra ICE Catheters Due to Potential Particle Contamination
FDA · Feb 25, 2026
FDA Recalls
Medline Industries Recalls Adult Catheter Securement Dressing Kits Due to Packaging Defect
FDA · Feb 25, 2026
FDA Recalls
Medline Industries Recalls Blood Culture Kits Over Potential Packaging Seal Breach
FDA · Feb 25, 2026
FDA Recalls high
Medline Industries Recalls Reprocessed Livewire Steerable Electrophysiology Catheters Due to Contamination Risk
FDA · Feb 25, 2026
FDA Recalls
Medline Industries Recalls Over 21,000 Medical Kits Due to Compromised Swabstick Packaging
FDA · Feb 25, 2026
FDA Recalls high
Medline Industries Recalls Reprocessed Biosense Webster Ultrasound Catheters Due to Potential Contamination
FDA · Feb 25, 2026
FDA Recalls
Medline Industries Recalls Sterile Resuture Packs Due to Potential Packaging Seal Defect
FDA · Feb 25, 2026
FDA Recalls
Surepulse Medical Ltd Recalls VS Cap Extra Large Over Labeling Error
FDA · Feb 25, 2026
FDA Recalls high
Medline Industries Recalls Adult Intubation Trays Over Life-Threatening Catheter Size Error
FDA · Feb 25, 2026
FDA Recalls
Surepulse Medical Ltd Recalls VS Cap Extra Small Due to Incorrect Sizing Labeling
FDA · Feb 25, 2026
FDA Recalls
Philips Recalls Azurion 5 M20 Systems Due to Unexpected Table Movement Hazard
FDA · Feb 25, 2026
FDA Recalls high
Elekta, Inc. Recalls Leksell GammaPlan Software Over Radiation Targeting Error
FDA · Feb 25, 2026
FDA Recalls
Medline Industries Recalls Medical Convenience Kits Due to BD ChloraPrep Packaging Defect
FDA · Feb 25, 2026
FDA Recalls
Steris Corporation Recalls Barco MNA with HexaVue IP Integration System Due to Configuration Error
FDA · Feb 25, 2026
FDA Recalls
Philips Medical Systems Recalls Azurion 7 B20 Systems Due to Unexpected Table Movement
FDA · Feb 25, 2026
FDA Recalls
Medline Industries Recalls Anesthesia Artline Packs Due to Potential Packaging Defect
FDA · Feb 25, 2026
FDA Recalls
SurePulse Medical Ltd Recalls Surepulse VS Cap Small Due to Labeling Error
FDA · Feb 25, 2026
FDA Recalls
Medline Recalls Suture Removal Trays Due to Potential Compromise of Sterile Packaging
FDA · Feb 25, 2026
FDA Recalls
Philips Medical Systems Recalls Azurion 3 M12 Systems Due to Unexpected Table Movement
FDA · Feb 25, 2026
FDA Recalls high
Medline Industries Recalls Reprocessed St. Jude Diagnostic Electrophysiology Catheters Due to Contamination Risk
FDA · Feb 25, 2026
FDA Recalls
Straumann USA LLC Recalls WB Impression Post Closed Trays Due to Component Mix-Up
FDA · Feb 25, 2026
FDA Recalls
Alphatec Spine Recalls ATEC Lateral Navigation Disc Prep Instruments Due to Design Flaw
FDA · Feb 25, 2026
FDA Recalls
Philips North America Recalls IQon Spectral CT Systems Due to Loose Fastener Risk
FDA · Feb 25, 2026
FDA Recalls
Philips Medical Systems Recalls Azurion 3 M15 Systems Due to Unexpected Table Movement
FDA · Feb 25, 2026
FDA Recalls
AVID Medical, Inc. Recalls Halyard TRANSPORT BAG KIT Over Potential Sterility Compromise
FDA · Feb 25, 2026
FDA Recalls
Philips Medical Systems Recalls Azurion 5 M12 Systems Over Unexpected Table Movement Hazard
FDA · Feb 25, 2026
FDA Recalls
Medline Industries Recalls Pediatric Catheter Securement Dressing Kits Over Sterility Concerns
FDA · Feb 25, 2026
FDA Recalls high
Intuitive Surgical Recalls da Vinci 5 Surgeon Console Viewer Displays Over Visualization Risks
FDA · Feb 25, 2026
FDA Recalls
Laerdal Medical Corporation Recalls Compact Suction Unit 4 Due to Electromagnetic Noise Interference
FDA · Feb 25, 2026
FDA Recalls high
Medline Industries Recalls Reprocessed Siemens ACUSON AcuNav Ultrasound Catheters Due to Contamination Risk
FDA · Feb 25, 2026
FDA Recalls
Philips Medical Systems Recalls Azurion 7 B12 Systems Due to Unexpected Table Movement
FDA · Feb 25, 2026
FDA Recalls high
Medline Industries Recalls Reprocessed Webster CS Catheters Due to Potential Residual Material
FDA · Feb 25, 2026
FDA Recalls
Philips Recalls Azurion 7 M20 Systems Due to Unexpected Table Movement
FDA · Feb 24, 2026
FDA Recalls high
Medline Industries Recalls 14 Fr Suction Catheter Kits Due to Incorrect Component Sizing
FDA · Feb 24, 2026
FDA Recalls
Philips Recalls Azurion 7 M12 Systems Due to Unexpected Table Movement Hazard
FDA · Feb 24, 2026
FDA Recalls high
Medline Industries Recalls Reprocessed Abbott Inquiry Steerable Diagnostic Catheters Due to Potential Contamination
FDA · Feb 24, 2026
FDA Recalls
Philips North America Recalls Spectral CT Systems Due to Potential Rotor Component Displacement
FDA · Feb 24, 2026
FDA Recalls high
Philips North America Recalls Brilliance iCT Systems Over Potential Projectile Hazard
FDA · Feb 24, 2026
FDA Recalls
SurePulse Medical Ltd Recalls Surepulse VS Cap Medium Over Incorrect Sizing Label
FDA · Feb 24, 2026
FDA Recalls
Medline Industries Recalls Medical Convenience Kits Due to Compromised Packaging Seals
FDA · Feb 24, 2026
FDA Recalls
Surepulse Medical Ltd Recalls VS Cap Large Due to Incorrect Labeling Sizing Guide
FDA · Feb 24, 2026
FDA Recalls high
Elekta, Inc. Recalls Leksell GammaPlan Software Due to Potential Incorrect Patient Irradiation Risk
FDA · Feb 24, 2026
FDA Recalls high
Carrot Top Kitchens Recalls White Truffle Hummus Due to Undeclared Sesame Allergen
FDA · Feb 24, 2026
FDA Recalls
Ventura Foods LLC Recalls Multiple Peanut Butter Brands Due to Potential Plastic Contamination
FDA · Feb 24, 2026
FDA Recalls
Karison Foods & Snacks Recalls Punjabi Pinni Due to Undeclared Milk Allergen
FDA · Feb 24, 2026
FDA Recalls high
Costco Recalls Kirkland Signature Mini Beignets Due to Undeclared Hazelnut
FDA · Feb 24, 2026
FDA Recalls high
McCain Foods USA Inc Recalls Ore-Ida Tater Tots Due to Plastic Fragments
FDA · Feb 24, 2026
FDA Recalls high
Karison Foods & Snacks, Inc. Recalls ALSI PINNI Due to Undeclared Milk Allergen
FDA · Feb 24, 2026
FDA Recalls
Red Button Movie House Popcorn Recall Issued Over Foreign Material Concerns
FDA · Feb 24, 2026
FDA Recalls high
Carrot Top Kitchens Recalls Lemon & Garlic Hummus Over Undeclared Sesame
FDA · Feb 24, 2026
FDA Recalls
McCain Foods USA Inc. Recalls Sonic Tots Due to Potential Plastic Contamination
FDA · Feb 24, 2026
FDA Recalls high
Karison Foods & Snacks Recalls Besan Laddoo Due to Undeclared Milk
FDA · Feb 24, 2026
FDA Recalls high
Island Crab Corporation Recalls Smoked Grouper Dip Over Undeclared Allergens
FDA · Feb 24, 2026
FDA Recalls
Ventura Foods LLC Recalls Poco Pac Peanut Butter and Jelly Packs Over Plastic Contamination
FDA · Feb 24, 2026
FDA Recalls high
TKS Co-pack Manufacturing Recalls Aonic Complete His Supplement Due to Potential Bacterial Contamination
FDA · Feb 24, 2026
FDA Recalls high
Carrot Top Kitchens Recalls Sundried Tomato and Caper Hummus Due to Undeclared Sesame
FDA · Feb 24, 2026
FDA Recalls
Ventura Foods LLC Recalls Poco Pac Peanut Butter and Strawberry Jam Due to Potential Plastic Contamination
FDA · Feb 24, 2026
FDA Recalls high
Carrot Top Kitchens Issues Recall for Cherry Pepper Hummus Due to Undeclared Sesame
FDA · Feb 24, 2026
FDA Recalls high
Karison Foods & Snacks Recalls Panjiri Due to Undeclared Milk Allergen
FDA · Feb 24, 2026
FDA Recalls high
Carrot Top Kitchens Recalls Lime Ginger Hummus Over Undeclared Sesame Allergen
FDA · Feb 24, 2026
FDA Recalls high
TKS Co-pack Manufacturing Recalls Aonic Complete Hers Supplement Shots Over Bacterial Contamination Concerns
FDA · Feb 24, 2026
FDA Recalls high
Cacao Art Recalls Crunchy Caramel Dark Chocolate Over Undeclared Milk Allergen
FDA · Feb 24, 2026
FDA Recalls
KPCM New York Inc. Recalls Preema Food Colour Powder Over Banned and Undeclared Additives
FDA · Feb 24, 2026
FDA Recalls
MG Foods Recalls Spicy Breakfast Burritos Due to Potential Plastic Fragments
FDA · Feb 24, 2026
FDA Recalls high
Asteria Health Recalls Testosterone and Anastrozole Sterile Pellets Due to Metal Particulate Matter
FDA · Feb 24, 2026
FDA Recalls
Pro Numb Tattoo Numbing Spray Recalled Nationwide Due to Manufacturing Deviations
FDA · Feb 24, 2026
FDA Recalls high
Asteria Health Recalls Estradiol Sterile Pellets Due to Potential Metal Contamination
FDA · Feb 24, 2026
FDA Recalls high
Asteria Health Recalls Estradiol 15 mg Sterile Pellets Due to Potential Metal Contamination
FDA · Feb 24, 2026
FDA Recalls high
Fresenius Kabi Compounding Recalls Acyclovir Sodium Injection Due to Sterility Concerns
FDA · Feb 24, 2026
FDA Recalls high
Asteria Health Recalls Testosterone and Anastrozole Sterile Pellets Due to Potential Metal Contamination
FDA · Feb 24, 2026
FDA Recalls
Unichem Pharmaceuticals Issues Nationwide Recall of Doxazosin Mesylate Tablets Due to Incorrect Imprint
FDA · Feb 24, 2026
FDA Recalls
Asteria Health Recalls Testosterone and Triamcinolone Acetonide Pellets Due to Potential Metal Contamination
FDA · Feb 24, 2026
FDA Recalls
Asteria Health Recalls Estradiol Sterile Pellets Due to Potential Metal Particulate Matter
FDA · Feb 24, 2026
FDA Recalls high
Asteria Health Recalls Testosterone Sterile Pellets Due to Potential Metal Contamination
FDA · Feb 24, 2026
FDA Recalls high
Fresenius Kabi Compounding Recalls Vancomycin HCl Injection Due to Sterility Concerns
FDA · Feb 24, 2026
FDA Recalls high
Asteria Health Issues Nationwide Recall of Estradiol Sterile Pellets Due to Metal Contamination Concerns
FDA · Feb 24, 2026
FDA Recalls high
Asteria Health Issues Nationwide Recall of Testosterone Sterile Pellets Due to Metal Particulates
FDA · Feb 24, 2026
FDA Recalls
American Health Packaging Recalls Oxycodone Hydrochloride Tablets Due to Defective Blister Seals
FDA · Feb 24, 2026
FDA Recalls high
Fresenius Kabi Compounding Recalls Ketamine HCl Injection Over Sterility Concerns
FDA · Feb 24, 2026
FDA Recalls high
Fresenius Kabi Compounding, LLC Recalls Thiamine HCl Injection Due to Lack of Sterility Assurance
FDA · Feb 24, 2026
FDA Recalls
Pro Numb Tattoo Numbing Spray Recalled Due to Manufacturing Deviations
FDA · Feb 24, 2026
FDA Recalls high
Asteria Health Recalls Testosterone Sterile Pellets Due to Potential Metal Particulate Matter
FDA · Feb 24, 2026
FDA Recalls
Changchun Wancheng Bio-Electron Recalls Vivoo Vaginal pH Tests Due to Lack of Marketing Clearance
FDA · Feb 19, 2026
FDA Recalls
Vortex Surgical Recalls Lindsell Sutured IOL Markers Over Sterility Concerns
FDA · Feb 19, 2026
FDA Recalls
Changchun Wancheng Bio-Electron Recalls Menopause Test Cassettes Over Regulatory Concerns
FDA · Feb 19, 2026
FDA Recalls high
Intuitive Surgical Recalls da Vinci X, Xi, and 5 Surgical Systems Due to Software Error
FDA · Feb 19, 2026
FDA Recalls
Fujirebio Diagnostics Recalls Lumipulse G pTau 217 Plasma Immunoreaction Cartridges Due to Inaccurate Results
FDA · Feb 19, 2026
FDA Recalls high
ETAC A/S Recalls Molift Mover 300 Mobile Hoists Due to Structural Component Failure
FDA · Feb 19, 2026
FDA Recalls
Wilson-Cook Medical Inc. Recalls Nasal Jejunal Feeding Tubes Due to Missing Components
FDA · Feb 19, 2026
FDA Recalls
Encore Medical Recalls EMPOWR Acetabular System Liners Due to Packaging Discrepancy
FDA · Feb 19, 2026
FDA Recalls high
Vortex Surgical Recalls Rumex Disposable Diamond Dusted ILM Elevator Over Sterility Concerns
FDA · Feb 19, 2026
FDA Recalls
Siemens Medical Solutions Recalls NAEOTOM Alpha.Prime Software Applications Over Lack of FDA Clearance
FDA · Feb 19, 2026
FDA Recalls high
ETAC A/S Recalls Molift 2-Point Sling Bars Due to Structural Bolt Failure Risk
FDA · Feb 19, 2026
FDA Recalls high
Vortex Surgical Recalls Volk Single Use Vitrectomy Lenses Due to Potential Sterility Breach
FDA · Feb 19, 2026
FDA Recalls
Maquet Cardiopulmonary Gmbh Recalls Bubble Sensors Over Cable Durability Concerns
FDA · Feb 19, 2026
FDA Recalls
Changchun Wancheng Bio-Electron Recalls LH One Step Ovulation Test Devices Over Lack of FDA Clearance
FDA · Feb 19, 2026
FDA Recalls high
Boston Scientific Recalls AXIOS Stent and Delivery Systems Over Deployment Failures
FDA · Feb 19, 2026
FDA Recalls high
Boston Scientific Recalls HOT AXIOS Stent Systems Due to Deployment and Expansion Issues
FDA · Feb 19, 2026
FDA Recalls
Olympus Recalls Single Use Sphincterotome V Due to Potential Performance Failure
FDA · Feb 19, 2026
FDA Recalls
Fujirebio Diagnostics Recalls Lumipulse G Beta-Amyloid 1-42-N Plasma Calibrators Due to Inaccurate Test Results
FDA · Feb 18, 2026
FDA Recalls high
Vortex Surgical Inc. Recalls Disposable Forceps and Cannulas Due to Potential Sterility Breach
FDA · Feb 18, 2026
FDA Recalls
Beckman Coulter Recalls CellMek SPS Sample Preparation System Due to Software Error
FDA · Feb 18, 2026
FDA Recalls high
Vortex Surgical Recalls 25GA Subretinal Injection Cannula Due to Potential Sterility Breach
FDA · Feb 18, 2026
FDA Recalls
Changchun Wancheng Bio-Electron Recalls Vivoo Sodium, Vitamin C, and Hydration Tests Due to Marketing Violations
FDA · Feb 18, 2026
FDA Recalls
Vivoo pH Test Recalled Due to Lack of Marketing Clearance and Risk of Inaccurate Results
FDA · Feb 18, 2026
FDA Recalls
Olympus Recalls Disposable Triple Lumen Sphincterotome Due to Potential Deformation and Performance Loss
FDA · Feb 18, 2026
FDA Recalls high
Changchun Wancheng Bio-Electron Recalls 32,500 Test Strips Over Marketing and Accuracy Concerns
FDA · Feb 18, 2026
FDA Recalls high
Vortex Surgical Inc. Recalls Tecfen Retractable Membrane Polisher Due to Sterility Concerns
FDA · Feb 18, 2026
FDA Recalls
Siemens Medical Solutions Recalls NAEOTOM Alpha Software Applications Over Missing FDA Clearance
FDA · Feb 18, 2026
FDA Recalls
Tornier, Inc. Recalls Reversed Peripheral Screws Due to Labeling Error
FDA · Feb 18, 2026
FDA Recalls
Fujirebio Diagnostics Recalls Lumipulse G β-Amyloid 1-42-N Plasma Test Cartridges for Inaccurate Results
FDA · Feb 18, 2026
FDA Recalls high
Vortex Surgical Recalls 25GA I.D.D. Internal Delivery Devices Over Sterility Risks
FDA · Feb 18, 2026
FDA Recalls
Changchun Wancheng Bio-Electron Recalls S. Typhi/Para Typhi A Antigen Test Strips Over Marketing Concerns
FDA · Feb 18, 2026
FDA Recalls high
Medtronic Recalls MiniMed 780G Insulin Pumps Due to Software Error Suspending Insulin Delivery
FDA · Feb 18, 2026
FDA Recalls high
Vortex Surgical Inc. Recalls Oertli Laser Probes Due to Potential Sterility Breach
FDA · Feb 18, 2026
FDA Recalls
Fujirebio Diagnostics Recalls Lumipulse β-Amyloid Plasma Controls Over Inaccurate Alzheimer's Test Results
FDA · Feb 18, 2026
FDA Recalls
Fujirebio Diagnostics Recalls Lumipulse G pTau217/B-Amyloid 1-42 Plasma Ratio Test Due to Inaccurate Results
FDA · Feb 18, 2026
FDA Recalls high
Olympus Recalls Single Use Electrosurgical Knife KD-645 Over Tip Breakage Concerns
FDA · Feb 18, 2026
FDA Recalls
Vantive US Healthcare Recalls Prismaflex ST150 Sets Due to Chamber Dislodgement Risk
FDA · Feb 18, 2026
FDA Recalls
Olympus Recalls Single Use Electrosurgical Knife KD-640L Due to Tip Breakage Risk
FDA · Feb 18, 2026
FDA Recalls high
Boston Scientific Recalls AXIOS Stent and Delivery System Over Deployment Failures
FDA · Feb 18, 2026
FDA Recalls
Siemens Medical Solutions Recalls SOMATOM X.ceed Software Applications Over Lack of FDA Clearance
FDA · Feb 18, 2026
FDA Recalls
Changchun Wancheng Bio-Electron Recalls Over 91,000 UTI and Urinalysis Test Strips Due to Inaccuracy Risk
FDA · Feb 18, 2026
FDA Recalls high
Encore Medical Recalls EMPOWR 3D Knee Tibial Inserts Over Packaging Errors
FDA · Feb 18, 2026
FDA Recalls
Siemens Medical Solutions Recalls NAEOTOM Alpha.Pro Software Applications Due to Lack of FDA Clearance
FDA · Feb 18, 2026
FDA Recalls high
Vantive US Healthcare Recalls Prismaflex HF1000 Sets Due to Component Dislodgement Risk
FDA · Feb 18, 2026
FDA Recalls
Vantive US Healthcare Recalls Prismaflex TPE2000 Sets Due to Component Dislodgement Risk
FDA · Feb 18, 2026
FDA Recalls
Vortex Surgical Recalls Backflush Devices Due to Potential Sterile Barrier Breach
FDA · Feb 18, 2026
FDA Recalls high
Vortex Surgical Recalls I2 Injection Kits Over Potential Sterility Breach
FDA · Feb 18, 2026
FDA Recalls
Olympus Recalls CleverCut Single Use 3-Lumen Sphincterotome V Over Performance Concerns
FDA · Feb 18, 2026
FDA Recalls
Olympus Corporation Recalls Disposable Triple Lumen Sphincterotomes Due to Potential Device Deformation
FDA · Feb 18, 2026
FDA Recalls
Vortex Surgical Recalls TID Pharos Illuminated Depressor Over Potential Safety Issues
FDA · Feb 18, 2026
FDA Recalls
Vantive US Healthcare Recalls PRISMAFLEX M150 Sets Due to Deaeration Chamber Issues
FDA · Feb 18, 2026
FDA Recalls high
Boston Scientific Recalls HOT AXIOS Stent and Delivery System Due to Deployment Failures
FDA · Feb 18, 2026
FDA Recalls
FUJIFILM Healthcare Recalls FDR Visionary Suite X-ray Systems Over Overheating and Smoke Risk
FDA · Feb 18, 2026
FDA Recalls high
Changchun Wancheng Bio-Electron Recalls Vivoo Protein Test Strips Over Marketing Clearance Issues
FDA · Feb 18, 2026
FDA Recalls high
Vortex Surgical Recalls Laser Probes Due to Potential Sterile Barrier Breach
FDA · Feb 18, 2026
FDA Recalls
Vantive US Healthcare Recalls Oxiris Set Dialyzers Due to Chamber Dislodgement Risk
FDA · Feb 18, 2026
FDA Recalls
Olympus Recalls Single Use 3-Lumen Sphincterotome V Over Performance Concerns
FDA · Feb 18, 2026
FDA Recalls
Vantive US Healthcare Recalls Prismaflex ST100 Sets Due to Chamber Dislodgement Risk
FDA · Feb 18, 2026
FDA Recalls high
Focalyx Technologies Recalls Focalyx Fusion Software Due to Windows 10 Compatibility Risks
FDA · Feb 18, 2026
FDA Recalls
Vantive US Healthcare Recalls Primsaflex M100 Set Due to Deaeration Chamber Dislodgement Risk
FDA · Feb 18, 2026
FDA Recalls
Olympus Recalls Disposable Triple Lumen Sphincterotome Due to Potential Device Deformation
FDA · Feb 18, 2026
FDA Recalls high
Boston Scientific Recalls AXIOS Stent and Delivery System Due to Deployment Risks
FDA · Feb 18, 2026
FDA Recalls high
Boston Scientific Recalls HOT AXIOS Stent and Delivery System Over Deployment Failures
FDA · Feb 18, 2026
FDA Recalls
Olympus Corporation Recalls Disposable Triple Lumen Sphincterotomes Over Performance Concerns
FDA · Feb 18, 2026
FDA Recalls
Fujirebio Diagnostics Recalls Lumipulse G pTau 217 Plasma Calibrators Due to Inaccurate Test Results
FDA · Feb 18, 2026
FDA Recalls high
ETAC A/S Recalls Molift Mover 205 Patient Lifts Due to Structural Bolt Failure
FDA · Feb 18, 2026
FDA Recalls
Olympus Recalls Single Use 3-Lumen Sphincterotome V Due to Device Deformation Risk
FDA · Feb 18, 2026
FDA Recalls
Exploro Male Fertility and Sperm Concentration Tests Recalled Due to Lack of FDA Clearance
FDA · Feb 17, 2026
FDA Recalls
Biomerieux Inc Recalls VITEK 2 Gram-negative Susceptibility Cards Due to Potential for False Test Results
FDA · Feb 17, 2026
FDA Recalls
Changchun Wancheng Bio-Electron Recalls Male Fertility Sperm Tests Due to Lack of FDA Clearance
FDA · Feb 17, 2026
FDA Recalls
Olympus Recalls Single Use 3-Lumen Sphincterotome V Due to Potential Device Deformation
FDA · Feb 17, 2026
FDA Recalls
Olympus Corporation Recalls Single Use 3-Lumen Sphincterotome V Due to Potential Performance Loss
FDA · Feb 17, 2026
FDA Recalls high
ETAC A/S Recalls Molift 4-Point Sling Bars Due to Risk of Structural Failure
FDA · Feb 17, 2026
FDA Recalls
Fujirebio Diagnostics Recalls Lumipulse pTau 217 Plasma Controls Over Inaccurate Alzheimer's Test Results
FDA · Feb 17, 2026
FDA Recalls
Olympus Recalls Disposable Triple Lumen Sphincterotomes Due to Potential Performance Loss
FDA · Feb 17, 2026
FDA Recalls
Olympus Recalls Single Use 3-Lumen Sphincterotome V Due to Potential Performance Loss
FDA · Feb 17, 2026
FDA Recalls
Beckman Coulter Recalls COULTER DxH Diluent Lots Due to Elevated Platelet Background Counts
FDA · Feb 17, 2026
FDA Recalls high
Vortex Surgical Inc. Recalls Convenience Kits Over Potential Sterility Breach
FDA · Feb 17, 2026
FDA Recalls high
Everpress Juice Recalls 'JUICE from the Raw, DETOX GREENS' Due to Potential Pathogenic Bacteria
FDA · Feb 17, 2026
FDA Recalls high
Everpress Juice Recalls 'JUICE from the Raw' Sweet Greens Due to Potential Pathogenic Bacteria
FDA · Feb 17, 2026
FDA Recalls
Prima Foods International Recalls BarbaCuban 455 Everything Sauce Due to Undeclared Quinine
FDA · Feb 17, 2026
FDA Recalls high
WinCo Foods Recalls Deli Margherita Pizza Due to Potential Metal Fragments
FDA · Feb 17, 2026
FDA Recalls
Organic Spices, Inc. Recalls Spicely Organic Celery Salt Due to Mislabeling and Salt Content
FDA · Feb 17, 2026
FDA Recalls high
Diva Fam Inc Recalls Sea Moss Gel Superfood Over Potential Botulism Contamination
FDA · Feb 17, 2026
FDA Recalls high
Venzu Traders LLC Recalls Cinnamon Powder Due to Potential Lead Contamination
FDA · Feb 17, 2026
FDA Recalls high
Everpress Juice Recalls 'JUICE from the Raw, upbeat' Due to Potential Pathogenic Bacteria
FDA · Feb 17, 2026
FDA Recalls
Organic Spices, Inc. Recalls Spicely Organic Sumac Due to Mislabeled Salt Content
FDA · Feb 17, 2026
FDA Recalls
Lost and Found Energy Sour Gummy Bear Recall Due to Incorrect Caffeine Labeling
FDA · Feb 17, 2026
FDA Recalls
Organic Spices, Inc. Recalls Spicely Organic Garlic Salt Due to Mislabeling Error
FDA · Feb 17, 2026
FDA Recalls
Prima Foods International Recalls BarbaCuban Mojo Marinade Over Undeclared Quinine
FDA · Feb 17, 2026
FDA Recalls
Optiwize Inc. Issues Voluntary Recall for OptiWize Collagen Plus Over Ingredient Discrepancy
FDA · Feb 17, 2026
FDA Recalls high
Beacon Promotions Inc Recalls Repackaged M&Ms Peanut Candies Due to Undeclared Allergens
FDA · Feb 17, 2026
FDA Recalls high
B.C. Williams Bakery Service, Inc. Recalls Bread and Roll Mix Due to Undeclared Milk Allergen
FDA · Feb 17, 2026
FDA Recalls high
B.C. Williams Bakery Service Recalls Spice Cake Mix Due to Undeclared Milk Allergen
FDA · Feb 17, 2026
FDA Recalls
Prima Foods International Recalls BarbaCuban Ram Air Red Zesty Ketchup Due to Undeclared Quinine
FDA · Feb 17, 2026
FDA Recalls
Prima Foods International Recalls BarbaCuban White Truffle Sauce Due to Undeclared Quinine
FDA · Feb 17, 2026
FDA Recalls high
Tradin Organics USA LLC Recalls Organic Black Chia Seeds Over Salmonella Concerns
FDA · Feb 17, 2026
FDA Recalls high
Everpress Juice Issues Recall for 'JUICE from the Raw' Spicy Lemonade Over Pathogen Risk
FDA · Feb 17, 2026
FDA Recalls
Prima Foods International Recalls BarbaCuban Havana Gold Due to Undeclared Quinine
FDA · Feb 17, 2026
FDA Recalls high
Everpress Juice Issues Recall for 'JUICE from the Raw' Pineapple Mint Over Pathogen Concerns
FDA · Feb 17, 2026
FDA Recalls high
B.C. Williams Bakery Service Recalls Swiss Chocolate Cake Mix Due to Undeclared Milk Allergen
FDA · Feb 17, 2026
FDA Recalls
Willy Pete's Chocolate Company LLC Recalls Almond Despair Chocolates Due to Labeling Error
FDA · Feb 17, 2026
FDA Recalls
Prima Foods International Recalls BarbaCuban 455 Everything Sauce Over Undeclared Quinine
FDA · Feb 17, 2026
FDA Recalls high
Everpress Juice Recalls 'JUICE from the Raw' Cashew Coffee Milk Over Bacterial Concerns
FDA · Feb 17, 2026
FDA Recalls high
Everpress Juice Issues Recall for 'JUICE from the Raw' Cashew Milk Over Bacterial Concerns
FDA · Feb 17, 2026
FDA Recalls high
Khee Trading Inc. Recalls Frozen Half Shell Oysters Due to Potential Norovirus Contamination
FDA · Feb 17, 2026
FDA Recalls high
Imu-Tek Animal Health Recalls Immuno-5 Colostrum Powder Due to Undeclared Milk Allergen
FDA · Feb 17, 2026
FDA Recalls high
Diva Fam Inc Recalls Mango Sea Moss Gel Superfood Over Potential Botulism Risk
FDA · Feb 17, 2026
FDA Recalls high
Outside The Breadbox Bread Crumbs Recalled Over Undeclared Egg and Milk
FDA · Feb 17, 2026
FDA Recalls high
Diva Fam Inc Recalls Sea Moss Gel Superfood Due to Potential Botulism Contamination
FDA · Feb 17, 2026
FDA Recalls high
Diva Fam Inc Recalls Sea Moss Gel Superfood Due to Potential Botulism Risk
FDA · Feb 17, 2026
FDA Recalls high
Tai Phat Wholesalers Recalls Sofit Seedless Red Dates Due to Undeclared Sulfites
FDA · Feb 17, 2026
FDA Recalls high
Beacon Promotions Inc Recalls Repackaged M&Ms Due to Undeclared Milk, Soy, and Peanut Allergens
FDA · Feb 17, 2026
FDA Recalls high
Diva Fam Inc Issues Nationwide Recall of Sea Moss Gel Superfood Over Botulism Concerns
FDA · Feb 17, 2026
FDA Recalls high
Handelnine Global LLC Recalls Rheumacare Capsules Due to Lead Contamination
FDA · Feb 17, 2026
FDA Recalls high
Granules Pharmaceuticals Inc. Recalls Trazodone Hydrochloride Due to Foreign Tablets
FDA · Feb 17, 2026
FDA Recalls high
Green Lumber Natural Fuel For Men Recall Issued Due to Undeclared Tadalafil
FDA · Feb 17, 2026
FDA Recalls high
Primavera Roasted Pumpkin & White Cheddar Tamales Recalled Due to Potential Listeria Contamination
FDA · Feb 11, 2026
FDA Recalls high
Hannaford Hamburger Dill Pickle Chips Recalled Due to Potential Glass Contamination
FDA · Feb 11, 2026
FDA Recalls high
Primavera BBQ Chipotle Bean & White Cheddar Tamales Recalled Due to Potential Listeria Contamination
FDA · Feb 11, 2026
FDA Recalls
New Way Import Inc. Recalls Preserved Mustard Over Undeclared Wheat Allergen
FDA · Feb 11, 2026
FDA Recalls
Weaver's Brew LLC Recalls Goldenroot Lemon Ginger Elderberry Ginger Beer Over Pasteurization Concerns
FDA · Feb 11, 2026
FDA Recalls high
Plant Based Innovations Recalls Higher Harvest by H-E-B Strawberry Yogurt Due to Undeclared Almonds
FDA · Feb 11, 2026
FDA Recalls
Weaver's Brew LLC Recalls Goldenroot Lemon Double Ginger Beer Due to Pasteurization Issue
FDA · Feb 11, 2026
FDA Recalls
Weaver's Brew LLC Recalls Goldenroot Ginger Beer Over Pasteurization Concerns
FDA · Feb 11, 2026
FDA Recalls high
Superfoods, Inc. Recalls Live it Up Super Greens Due to Potential Salmonella Contamination
FDA · Feb 11, 2026
FDA Recalls high
Primavera Roasted Green Chile Tamales Recalled Due to Potential Listeria Contamination
FDA · Feb 11, 2026
FDA Recalls
Keurig Dr Pepper Recalls McCafe Decaf K-Cup Pods Due to Potential Caffeine Content
FDA · Feb 11, 2026
FDA Recalls high
Prima Vera Nueva, Inc. Recalls Black Bean Bonanza Tamales Due to Potential Listeria Contamination
FDA · Feb 11, 2026
FDA Recalls high
Primavera Black Bean Bonanza Tamales Recalled Due to Potential Listeria Contamination
FDA · Feb 11, 2026
FDA Recalls high
Primavera Recalls Butternut Squash Tamales Due to Potential Listeria Contamination
FDA · Feb 11, 2026
FDA Recalls high
Prima Vera Nueva, Inc. Recalls Butternut Squash Tamales Over Listeria Concerns
FDA · Feb 11, 2026
FDA Recalls
Goldenroot Lemon Ginger Jalapeno Ginger Beer Recalled Over Pasteurization Concerns
FDA · Feb 11, 2026
FDA Recalls high
Prima Vera Nueva, Inc. Recalls Roasted Green Chile & Jack Cheese Tamales Due to Potential Listeria Contamination
FDA · Feb 11, 2026
FDA Recalls high
Prima Vera Nueva, Inc. Recalls Mushroom, Spinach & Salsa Tamales Due to Potential Listeria Contamination
FDA · Feb 11, 2026
FDA Recalls high
Bharat Bazar Recalls Soma Kitchen Natural Asafoetida Due to Undeclared Wheat
FDA · Feb 11, 2026
FDA Recalls
Sato Pharmaceutical Recalls INON ACE Antacid Tablets Due to Disintegration Failure
FDA · Feb 11, 2026
FDA Recalls
Greenstone LLC Recalls Methylprednisolone Dosepak Tablets Due to Dosing Labeling Error
FDA · Feb 11, 2026
FDA Recalls
Novadoz Pharmaceuticals LLC Recalls Glycopyrrolate Oral Solution Due to Impurity Specifications
FDA · Feb 11, 2026
FDA Recalls
Baxter Healthcare Recalls Sterile Water for Irrigation Due to Plastic Particulate Matter
FDA · Feb 11, 2026
FDA Recalls
Haleon US Holdings LLC Recalls Parodontax Active Gum Health Mouthwash Due to Labeling Issues
FDA · Feb 11, 2026