FDA Recalls - February 2026 (225 reports)
FDA Recalls issued during February 2026.
FDA Recalls
Philips North America Recalls Spectral CT 7500 on Rails Over Potential Rotor Part Displacement
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FDA Recalls
Medline Industries Recalls Mercy Circumcision Trays Due to Compromised Packaging
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FDA Recalls high
Medline Industries Recalls Reprocessed ViewFlex Xtra ICE Catheters Due to Potential Particle Contamination
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FDA Recalls
Medline Industries Recalls Adult Catheter Securement Dressing Kits Due to Packaging Defect
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FDA Recalls
Medline Industries Recalls Blood Culture Kits Over Potential Packaging Seal Breach
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FDA Recalls high
Medline Industries Recalls Reprocessed Livewire Steerable Electrophysiology Catheters Due to Contamination Risk
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FDA Recalls
Medline Industries Recalls Over 21,000 Medical Kits Due to Compromised Swabstick Packaging
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FDA Recalls high
Medline Industries Recalls Reprocessed Biosense Webster Ultrasound Catheters Due to Potential Contamination
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FDA Recalls
Medline Industries Recalls Sterile Resuture Packs Due to Potential Packaging Seal Defect
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FDA Recalls
Surepulse Medical Ltd Recalls VS Cap Extra Large Over Labeling Error
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FDA Recalls high
Medline Industries Recalls Adult Intubation Trays Over Life-Threatening Catheter Size Error
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FDA Recalls
Surepulse Medical Ltd Recalls VS Cap Extra Small Due to Incorrect Sizing Labeling
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FDA Recalls
Philips Recalls Azurion 5 M20 Systems Due to Unexpected Table Movement Hazard
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FDA Recalls high
Elekta, Inc. Recalls Leksell GammaPlan Software Over Radiation Targeting Error
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FDA Recalls
Medline Industries Recalls Medical Convenience Kits Due to BD ChloraPrep Packaging Defect
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FDA Recalls
Steris Corporation Recalls Barco MNA with HexaVue IP Integration System Due to Configuration Error
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FDA Recalls
Philips Medical Systems Recalls Azurion 7 B20 Systems Due to Unexpected Table Movement
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FDA Recalls
Medline Industries Recalls Anesthesia Artline Packs Due to Potential Packaging Defect
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FDA Recalls
SurePulse Medical Ltd Recalls Surepulse VS Cap Small Due to Labeling Error
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FDA Recalls
Medline Recalls Suture Removal Trays Due to Potential Compromise of Sterile Packaging
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FDA Recalls
Philips Medical Systems Recalls Azurion 3 M12 Systems Due to Unexpected Table Movement
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FDA Recalls high
Medline Industries Recalls Reprocessed St. Jude Diagnostic Electrophysiology Catheters Due to Contamination Risk
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FDA Recalls
Straumann USA LLC Recalls WB Impression Post Closed Trays Due to Component Mix-Up
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FDA Recalls
Alphatec Spine Recalls ATEC Lateral Navigation Disc Prep Instruments Due to Design Flaw
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FDA Recalls
Philips North America Recalls IQon Spectral CT Systems Due to Loose Fastener Risk
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FDA Recalls
Philips Medical Systems Recalls Azurion 3 M15 Systems Due to Unexpected Table Movement
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FDA Recalls
AVID Medical, Inc. Recalls Halyard TRANSPORT BAG KIT Over Potential Sterility Compromise
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FDA Recalls
Philips Medical Systems Recalls Azurion 5 M12 Systems Over Unexpected Table Movement Hazard
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FDA Recalls
Medline Industries Recalls Pediatric Catheter Securement Dressing Kits Over Sterility Concerns
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FDA Recalls high
Intuitive Surgical Recalls da Vinci 5 Surgeon Console Viewer Displays Over Visualization Risks
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FDA Recalls
Laerdal Medical Corporation Recalls Compact Suction Unit 4 Due to Electromagnetic Noise Interference
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FDA Recalls high
Medline Industries Recalls Reprocessed Siemens ACUSON AcuNav Ultrasound Catheters Due to Contamination Risk
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FDA Recalls
Philips Medical Systems Recalls Azurion 7 B12 Systems Due to Unexpected Table Movement
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FDA Recalls high
Medline Industries Recalls Reprocessed Webster CS Catheters Due to Potential Residual Material
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FDA Recalls
Philips Recalls Azurion 7 M20 Systems Due to Unexpected Table Movement
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FDA Recalls high
Medline Industries Recalls 14 Fr Suction Catheter Kits Due to Incorrect Component Sizing
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FDA Recalls
Philips Recalls Azurion 7 M12 Systems Due to Unexpected Table Movement Hazard
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FDA Recalls high
Medline Industries Recalls Reprocessed Abbott Inquiry Steerable Diagnostic Catheters Due to Potential Contamination
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FDA Recalls
Philips North America Recalls Spectral CT Systems Due to Potential Rotor Component Displacement
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FDA Recalls high
Philips North America Recalls Brilliance iCT Systems Over Potential Projectile Hazard
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FDA Recalls
SurePulse Medical Ltd Recalls Surepulse VS Cap Medium Over Incorrect Sizing Label
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FDA Recalls
Medline Industries Recalls Medical Convenience Kits Due to Compromised Packaging Seals
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FDA Recalls
Surepulse Medical Ltd Recalls VS Cap Large Due to Incorrect Labeling Sizing Guide
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FDA Recalls high
Elekta, Inc. Recalls Leksell GammaPlan Software Due to Potential Incorrect Patient Irradiation Risk
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FDA Recalls high
Carrot Top Kitchens Recalls White Truffle Hummus Due to Undeclared Sesame Allergen
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FDA Recalls
Ventura Foods LLC Recalls Multiple Peanut Butter Brands Due to Potential Plastic Contamination
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FDA Recalls
Karison Foods & Snacks Recalls Punjabi Pinni Due to Undeclared Milk Allergen
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FDA Recalls high
Costco Recalls Kirkland Signature Mini Beignets Due to Undeclared Hazelnut
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FDA Recalls high
McCain Foods USA Inc Recalls Ore-Ida Tater Tots Due to Plastic Fragments
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FDA Recalls high
Karison Foods & Snacks, Inc. Recalls ALSI PINNI Due to Undeclared Milk Allergen
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FDA Recalls
Red Button Movie House Popcorn Recall Issued Over Foreign Material Concerns
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FDA Recalls high
Carrot Top Kitchens Recalls Lemon & Garlic Hummus Over Undeclared Sesame
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FDA Recalls
McCain Foods USA Inc. Recalls Sonic Tots Due to Potential Plastic Contamination
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FDA Recalls high
Karison Foods & Snacks Recalls Besan Laddoo Due to Undeclared Milk
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FDA Recalls high
Island Crab Corporation Recalls Smoked Grouper Dip Over Undeclared Allergens
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FDA Recalls
Ventura Foods LLC Recalls Poco Pac Peanut Butter and Jelly Packs Over Plastic Contamination
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FDA Recalls high
TKS Co-pack Manufacturing Recalls Aonic Complete His Supplement Due to Potential Bacterial Contamination
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FDA Recalls high
Carrot Top Kitchens Recalls Sundried Tomato and Caper Hummus Due to Undeclared Sesame
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FDA Recalls
Ventura Foods LLC Recalls Poco Pac Peanut Butter and Strawberry Jam Due to Potential Plastic Contamination
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FDA Recalls high
Carrot Top Kitchens Issues Recall for Cherry Pepper Hummus Due to Undeclared Sesame
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FDA Recalls high
Karison Foods & Snacks Recalls Panjiri Due to Undeclared Milk Allergen
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FDA Recalls high
Carrot Top Kitchens Recalls Lime Ginger Hummus Over Undeclared Sesame Allergen
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FDA Recalls high
TKS Co-pack Manufacturing Recalls Aonic Complete Hers Supplement Shots Over Bacterial Contamination Concerns
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FDA Recalls high
Cacao Art Recalls Crunchy Caramel Dark Chocolate Over Undeclared Milk Allergen
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FDA Recalls
KPCM New York Inc. Recalls Preema Food Colour Powder Over Banned and Undeclared Additives
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FDA Recalls
MG Foods Recalls Spicy Breakfast Burritos Due to Potential Plastic Fragments
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FDA Recalls high
Asteria Health Recalls Testosterone and Anastrozole Sterile Pellets Due to Metal Particulate Matter
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FDA Recalls
Pro Numb Tattoo Numbing Spray Recalled Nationwide Due to Manufacturing Deviations
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FDA Recalls high
Asteria Health Recalls Estradiol Sterile Pellets Due to Potential Metal Contamination
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FDA Recalls high
Asteria Health Recalls Estradiol 15 mg Sterile Pellets Due to Potential Metal Contamination
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FDA Recalls high
Fresenius Kabi Compounding Recalls Acyclovir Sodium Injection Due to Sterility Concerns
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FDA Recalls high
Asteria Health Recalls Testosterone and Anastrozole Sterile Pellets Due to Potential Metal Contamination
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FDA Recalls
Unichem Pharmaceuticals Issues Nationwide Recall of Doxazosin Mesylate Tablets Due to Incorrect Imprint
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FDA Recalls
Asteria Health Recalls Testosterone and Triamcinolone Acetonide Pellets Due to Potential Metal Contamination
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FDA Recalls
Asteria Health Recalls Estradiol Sterile Pellets Due to Potential Metal Particulate Matter
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FDA Recalls high
Asteria Health Recalls Testosterone Sterile Pellets Due to Potential Metal Contamination
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FDA Recalls high
Fresenius Kabi Compounding Recalls Vancomycin HCl Injection Due to Sterility Concerns
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FDA Recalls high
Asteria Health Issues Nationwide Recall of Estradiol Sterile Pellets Due to Metal Contamination Concerns
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FDA Recalls high
Asteria Health Issues Nationwide Recall of Testosterone Sterile Pellets Due to Metal Particulates
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FDA Recalls
American Health Packaging Recalls Oxycodone Hydrochloride Tablets Due to Defective Blister Seals
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FDA Recalls high
Fresenius Kabi Compounding Recalls Ketamine HCl Injection Over Sterility Concerns
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FDA Recalls high
Fresenius Kabi Compounding, LLC Recalls Thiamine HCl Injection Due to Lack of Sterility Assurance
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FDA Recalls
Pro Numb Tattoo Numbing Spray Recalled Due to Manufacturing Deviations
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FDA Recalls high
Asteria Health Recalls Testosterone Sterile Pellets Due to Potential Metal Particulate Matter
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FDA Recalls
Changchun Wancheng Bio-Electron Recalls Vivoo Vaginal pH Tests Due to Lack of Marketing Clearance
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FDA Recalls
Vortex Surgical Recalls Lindsell Sutured IOL Markers Over Sterility Concerns
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FDA Recalls
Changchun Wancheng Bio-Electron Recalls Menopause Test Cassettes Over Regulatory Concerns
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FDA Recalls high
Intuitive Surgical Recalls da Vinci X, Xi, and 5 Surgical Systems Due to Software Error
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FDA Recalls
Fujirebio Diagnostics Recalls Lumipulse G pTau 217 Plasma Immunoreaction Cartridges Due to Inaccurate Results
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FDA Recalls high
ETAC A/S Recalls Molift Mover 300 Mobile Hoists Due to Structural Component Failure
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FDA Recalls
Wilson-Cook Medical Inc. Recalls Nasal Jejunal Feeding Tubes Due to Missing Components
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FDA Recalls
Encore Medical Recalls EMPOWR Acetabular System Liners Due to Packaging Discrepancy
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FDA Recalls high
Vortex Surgical Recalls Rumex Disposable Diamond Dusted ILM Elevator Over Sterility Concerns
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FDA Recalls
Siemens Medical Solutions Recalls NAEOTOM Alpha.Prime Software Applications Over Lack of FDA Clearance
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FDA Recalls high
ETAC A/S Recalls Molift 2-Point Sling Bars Due to Structural Bolt Failure Risk
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FDA Recalls high
Vortex Surgical Recalls Volk Single Use Vitrectomy Lenses Due to Potential Sterility Breach
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FDA Recalls
Maquet Cardiopulmonary Gmbh Recalls Bubble Sensors Over Cable Durability Concerns
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FDA Recalls
Changchun Wancheng Bio-Electron Recalls LH One Step Ovulation Test Devices Over Lack of FDA Clearance
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FDA Recalls high
Boston Scientific Recalls AXIOS Stent and Delivery Systems Over Deployment Failures
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FDA Recalls high
Boston Scientific Recalls HOT AXIOS Stent Systems Due to Deployment and Expansion Issues
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FDA Recalls
Olympus Recalls Single Use Sphincterotome V Due to Potential Performance Failure
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FDA Recalls
Fujirebio Diagnostics Recalls Lumipulse G Beta-Amyloid 1-42-N Plasma Calibrators Due to Inaccurate Test Results
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FDA Recalls high
Vortex Surgical Inc. Recalls Disposable Forceps and Cannulas Due to Potential Sterility Breach
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FDA Recalls
Beckman Coulter Recalls CellMek SPS Sample Preparation System Due to Software Error
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FDA Recalls high
Vortex Surgical Recalls 25GA Subretinal Injection Cannula Due to Potential Sterility Breach
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FDA Recalls
Changchun Wancheng Bio-Electron Recalls Vivoo Sodium, Vitamin C, and Hydration Tests Due to Marketing Violations
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FDA Recalls
Vivoo pH Test Recalled Due to Lack of Marketing Clearance and Risk of Inaccurate Results
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FDA Recalls
Olympus Recalls Disposable Triple Lumen Sphincterotome Due to Potential Deformation and Performance Loss
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FDA Recalls high
Changchun Wancheng Bio-Electron Recalls 32,500 Test Strips Over Marketing and Accuracy Concerns
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FDA Recalls high
Vortex Surgical Inc. Recalls Tecfen Retractable Membrane Polisher Due to Sterility Concerns
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FDA Recalls
Siemens Medical Solutions Recalls NAEOTOM Alpha Software Applications Over Missing FDA Clearance
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FDA Recalls
Tornier, Inc. Recalls Reversed Peripheral Screws Due to Labeling Error
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FDA Recalls
Fujirebio Diagnostics Recalls Lumipulse G β-Amyloid 1-42-N Plasma Test Cartridges for Inaccurate Results
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FDA Recalls high
Vortex Surgical Recalls 25GA I.D.D. Internal Delivery Devices Over Sterility Risks
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FDA Recalls
Changchun Wancheng Bio-Electron Recalls S. Typhi/Para Typhi A Antigen Test Strips Over Marketing Concerns
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FDA Recalls high
Medtronic Recalls MiniMed 780G Insulin Pumps Due to Software Error Suspending Insulin Delivery
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FDA Recalls high
Vortex Surgical Inc. Recalls Oertli Laser Probes Due to Potential Sterility Breach
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FDA Recalls
Fujirebio Diagnostics Recalls Lumipulse β-Amyloid Plasma Controls Over Inaccurate Alzheimer's Test Results
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FDA Recalls
Fujirebio Diagnostics Recalls Lumipulse G pTau217/B-Amyloid 1-42 Plasma Ratio Test Due to Inaccurate Results
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FDA Recalls high
Olympus Recalls Single Use Electrosurgical Knife KD-645 Over Tip Breakage Concerns
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FDA Recalls
Vantive US Healthcare Recalls Prismaflex ST150 Sets Due to Chamber Dislodgement Risk
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FDA Recalls
Olympus Recalls Single Use Electrosurgical Knife KD-640L Due to Tip Breakage Risk
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FDA Recalls high
Boston Scientific Recalls AXIOS Stent and Delivery System Over Deployment Failures
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FDA Recalls
Siemens Medical Solutions Recalls SOMATOM X.ceed Software Applications Over Lack of FDA Clearance
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FDA Recalls
Changchun Wancheng Bio-Electron Recalls Over 91,000 UTI and Urinalysis Test Strips Due to Inaccuracy Risk
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FDA Recalls high
Encore Medical Recalls EMPOWR 3D Knee Tibial Inserts Over Packaging Errors
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FDA Recalls
Siemens Medical Solutions Recalls NAEOTOM Alpha.Pro Software Applications Due to Lack of FDA Clearance
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FDA Recalls high
Vantive US Healthcare Recalls Prismaflex HF1000 Sets Due to Component Dislodgement Risk
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FDA Recalls
Vantive US Healthcare Recalls Prismaflex TPE2000 Sets Due to Component Dislodgement Risk
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FDA Recalls
Vortex Surgical Recalls Backflush Devices Due to Potential Sterile Barrier Breach
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FDA Recalls high
Vortex Surgical Recalls I2 Injection Kits Over Potential Sterility Breach
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FDA Recalls
Olympus Recalls CleverCut Single Use 3-Lumen Sphincterotome V Over Performance Concerns
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FDA Recalls
Olympus Corporation Recalls Disposable Triple Lumen Sphincterotomes Due to Potential Device Deformation
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FDA Recalls
Vortex Surgical Recalls TID Pharos Illuminated Depressor Over Potential Safety Issues
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FDA Recalls
Vantive US Healthcare Recalls PRISMAFLEX M150 Sets Due to Deaeration Chamber Issues
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FDA Recalls high
Boston Scientific Recalls HOT AXIOS Stent and Delivery System Due to Deployment Failures
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FDA Recalls
FUJIFILM Healthcare Recalls FDR Visionary Suite X-ray Systems Over Overheating and Smoke Risk
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FDA Recalls high
Changchun Wancheng Bio-Electron Recalls Vivoo Protein Test Strips Over Marketing Clearance Issues
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FDA Recalls high
Vortex Surgical Recalls Laser Probes Due to Potential Sterile Barrier Breach
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FDA Recalls
Vantive US Healthcare Recalls Oxiris Set Dialyzers Due to Chamber Dislodgement Risk
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FDA Recalls
Olympus Recalls Single Use 3-Lumen Sphincterotome V Over Performance Concerns
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FDA Recalls
Vantive US Healthcare Recalls Prismaflex ST100 Sets Due to Chamber Dislodgement Risk
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FDA Recalls high
Focalyx Technologies Recalls Focalyx Fusion Software Due to Windows 10 Compatibility Risks
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FDA Recalls
Vantive US Healthcare Recalls Primsaflex M100 Set Due to Deaeration Chamber Dislodgement Risk
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FDA Recalls
Olympus Recalls Disposable Triple Lumen Sphincterotome Due to Potential Device Deformation
FDA ·
FDA Recalls high
Boston Scientific Recalls AXIOS Stent and Delivery System Due to Deployment Risks
FDA ·
FDA Recalls high
Boston Scientific Recalls HOT AXIOS Stent and Delivery System Over Deployment Failures
FDA ·
FDA Recalls
Olympus Corporation Recalls Disposable Triple Lumen Sphincterotomes Over Performance Concerns
FDA ·
FDA Recalls
Fujirebio Diagnostics Recalls Lumipulse G pTau 217 Plasma Calibrators Due to Inaccurate Test Results
FDA ·
FDA Recalls high
ETAC A/S Recalls Molift Mover 205 Patient Lifts Due to Structural Bolt Failure
FDA ·
FDA Recalls
Olympus Recalls Single Use 3-Lumen Sphincterotome V Due to Device Deformation Risk
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FDA Recalls
Exploro Male Fertility and Sperm Concentration Tests Recalled Due to Lack of FDA Clearance
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FDA Recalls
Biomerieux Inc Recalls VITEK 2 Gram-negative Susceptibility Cards Due to Potential for False Test Results
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FDA Recalls
Changchun Wancheng Bio-Electron Recalls Male Fertility Sperm Tests Due to Lack of FDA Clearance
FDA ·
FDA Recalls
Olympus Recalls Single Use 3-Lumen Sphincterotome V Due to Potential Device Deformation
FDA ·
FDA Recalls
Olympus Corporation Recalls Single Use 3-Lumen Sphincterotome V Due to Potential Performance Loss
FDA ·
FDA Recalls high
ETAC A/S Recalls Molift 4-Point Sling Bars Due to Risk of Structural Failure
FDA ·
FDA Recalls
Fujirebio Diagnostics Recalls Lumipulse pTau 217 Plasma Controls Over Inaccurate Alzheimer's Test Results
FDA ·
FDA Recalls
Olympus Recalls Disposable Triple Lumen Sphincterotomes Due to Potential Performance Loss
FDA ·
FDA Recalls
Olympus Recalls Single Use 3-Lumen Sphincterotome V Due to Potential Performance Loss
FDA ·
FDA Recalls
Beckman Coulter Recalls COULTER DxH Diluent Lots Due to Elevated Platelet Background Counts
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FDA Recalls high
Vortex Surgical Inc. Recalls Convenience Kits Over Potential Sterility Breach
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FDA Recalls high
Everpress Juice Recalls 'JUICE from the Raw, DETOX GREENS' Due to Potential Pathogenic Bacteria
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FDA Recalls high
Everpress Juice Recalls 'JUICE from the Raw' Sweet Greens Due to Potential Pathogenic Bacteria
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FDA Recalls
Prima Foods International Recalls BarbaCuban 455 Everything Sauce Due to Undeclared Quinine
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FDA Recalls high
WinCo Foods Recalls Deli Margherita Pizza Due to Potential Metal Fragments
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FDA Recalls
Organic Spices, Inc. Recalls Spicely Organic Celery Salt Due to Mislabeling and Salt Content
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FDA Recalls high
Diva Fam Inc Recalls Sea Moss Gel Superfood Over Potential Botulism Contamination
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FDA Recalls high
Venzu Traders LLC Recalls Cinnamon Powder Due to Potential Lead Contamination
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FDA Recalls high
Everpress Juice Recalls 'JUICE from the Raw, upbeat' Due to Potential Pathogenic Bacteria
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FDA Recalls
Organic Spices, Inc. Recalls Spicely Organic Sumac Due to Mislabeled Salt Content
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FDA Recalls
Lost and Found Energy Sour Gummy Bear Recall Due to Incorrect Caffeine Labeling
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FDA Recalls
Organic Spices, Inc. Recalls Spicely Organic Garlic Salt Due to Mislabeling Error
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FDA Recalls
Prima Foods International Recalls BarbaCuban Mojo Marinade Over Undeclared Quinine
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FDA Recalls
Optiwize Inc. Issues Voluntary Recall for OptiWize Collagen Plus Over Ingredient Discrepancy
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FDA Recalls high
Beacon Promotions Inc Recalls Repackaged M&Ms Peanut Candies Due to Undeclared Allergens
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FDA Recalls high
B.C. Williams Bakery Service, Inc. Recalls Bread and Roll Mix Due to Undeclared Milk Allergen
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FDA Recalls high
B.C. Williams Bakery Service Recalls Spice Cake Mix Due to Undeclared Milk Allergen
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FDA Recalls
Prima Foods International Recalls BarbaCuban Ram Air Red Zesty Ketchup Due to Undeclared Quinine
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FDA Recalls
Prima Foods International Recalls BarbaCuban White Truffle Sauce Due to Undeclared Quinine
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FDA Recalls high
Tradin Organics USA LLC Recalls Organic Black Chia Seeds Over Salmonella Concerns
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FDA Recalls high
Everpress Juice Issues Recall for 'JUICE from the Raw' Spicy Lemonade Over Pathogen Risk
FDA ·
FDA Recalls
Prima Foods International Recalls BarbaCuban Havana Gold Due to Undeclared Quinine
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FDA Recalls high
Everpress Juice Issues Recall for 'JUICE from the Raw' Pineapple Mint Over Pathogen Concerns
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FDA Recalls high
B.C. Williams Bakery Service Recalls Swiss Chocolate Cake Mix Due to Undeclared Milk Allergen
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FDA Recalls
Willy Pete's Chocolate Company LLC Recalls Almond Despair Chocolates Due to Labeling Error
FDA ·
FDA Recalls
Prima Foods International Recalls BarbaCuban 455 Everything Sauce Over Undeclared Quinine
FDA ·
FDA Recalls high
Everpress Juice Recalls 'JUICE from the Raw' Cashew Coffee Milk Over Bacterial Concerns
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FDA Recalls high
Everpress Juice Issues Recall for 'JUICE from the Raw' Cashew Milk Over Bacterial Concerns
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FDA Recalls high
Khee Trading Inc. Recalls Frozen Half Shell Oysters Due to Potential Norovirus Contamination
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FDA Recalls high
Imu-Tek Animal Health Recalls Immuno-5 Colostrum Powder Due to Undeclared Milk Allergen
FDA ·
FDA Recalls high
Diva Fam Inc Recalls Mango Sea Moss Gel Superfood Over Potential Botulism Risk
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FDA Recalls high
Outside The Breadbox Bread Crumbs Recalled Over Undeclared Egg and Milk
FDA ·
FDA Recalls high
Diva Fam Inc Recalls Sea Moss Gel Superfood Due to Potential Botulism Contamination
FDA ·
FDA Recalls high
Diva Fam Inc Recalls Sea Moss Gel Superfood Due to Potential Botulism Risk
FDA ·
FDA Recalls high
Tai Phat Wholesalers Recalls Sofit Seedless Red Dates Due to Undeclared Sulfites
FDA ·
FDA Recalls high
Beacon Promotions Inc Recalls Repackaged M&Ms Due to Undeclared Milk, Soy, and Peanut Allergens
FDA ·
FDA Recalls high
Diva Fam Inc Issues Nationwide Recall of Sea Moss Gel Superfood Over Botulism Concerns
FDA ·
FDA Recalls high
Handelnine Global LLC Recalls Rheumacare Capsules Due to Lead Contamination
FDA ·
FDA Recalls high
Granules Pharmaceuticals Inc. Recalls Trazodone Hydrochloride Due to Foreign Tablets
FDA ·
FDA Recalls high
Green Lumber Natural Fuel For Men Recall Issued Due to Undeclared Tadalafil
FDA ·
FDA Recalls high
Primavera Roasted Pumpkin & White Cheddar Tamales Recalled Due to Potential Listeria Contamination
FDA ·
FDA Recalls high
Hannaford Hamburger Dill Pickle Chips Recalled Due to Potential Glass Contamination
FDA ·
FDA Recalls high
Primavera BBQ Chipotle Bean & White Cheddar Tamales Recalled Due to Potential Listeria Contamination
FDA ·
FDA Recalls
New Way Import Inc. Recalls Preserved Mustard Over Undeclared Wheat Allergen
FDA ·
FDA Recalls
Weaver's Brew LLC Recalls Goldenroot Lemon Ginger Elderberry Ginger Beer Over Pasteurization Concerns
FDA ·
FDA Recalls high
Plant Based Innovations Recalls Higher Harvest by H-E-B Strawberry Yogurt Due to Undeclared Almonds
FDA ·
FDA Recalls
Weaver's Brew LLC Recalls Goldenroot Lemon Double Ginger Beer Due to Pasteurization Issue
FDA ·
FDA Recalls
Weaver's Brew LLC Recalls Goldenroot Ginger Beer Over Pasteurization Concerns
FDA ·
FDA Recalls high
Superfoods, Inc. Recalls Live it Up Super Greens Due to Potential Salmonella Contamination
FDA ·
FDA Recalls high
Primavera Roasted Green Chile Tamales Recalled Due to Potential Listeria Contamination
FDA ·
FDA Recalls
Keurig Dr Pepper Recalls McCafe Decaf K-Cup Pods Due to Potential Caffeine Content
FDA ·
FDA Recalls high
Prima Vera Nueva, Inc. Recalls Black Bean Bonanza Tamales Due to Potential Listeria Contamination
FDA ·
FDA Recalls high
Primavera Black Bean Bonanza Tamales Recalled Due to Potential Listeria Contamination
FDA ·
FDA Recalls high
Primavera Recalls Butternut Squash Tamales Due to Potential Listeria Contamination
FDA ·
FDA Recalls high
Prima Vera Nueva, Inc. Recalls Butternut Squash Tamales Over Listeria Concerns
FDA ·
FDA Recalls
Goldenroot Lemon Ginger Jalapeno Ginger Beer Recalled Over Pasteurization Concerns
FDA ·
FDA Recalls high
Prima Vera Nueva, Inc. Recalls Roasted Green Chile & Jack Cheese Tamales Due to Potential Listeria Contamination
FDA ·
FDA Recalls high
Prima Vera Nueva, Inc. Recalls Mushroom, Spinach & Salsa Tamales Due to Potential Listeria Contamination
FDA ·
FDA Recalls high
Bharat Bazar Recalls Soma Kitchen Natural Asafoetida Due to Undeclared Wheat
FDA ·
FDA Recalls
Sato Pharmaceutical Recalls INON ACE Antacid Tablets Due to Disintegration Failure
FDA ·
FDA Recalls
Greenstone LLC Recalls Methylprednisolone Dosepak Tablets Due to Dosing Labeling Error
FDA ·
FDA Recalls
Novadoz Pharmaceuticals LLC Recalls Glycopyrrolate Oral Solution Due to Impurity Specifications
FDA ·
FDA Recalls
Baxter Healthcare Recalls Sterile Water for Irrigation Due to Plastic Particulate Matter
FDA ·
FDA Recalls
Haleon US Holdings LLC Recalls Parodontax Active Gum Health Mouthwash Due to Labeling Issues
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All federal data sources used on this page
- FDA Enforcement Report - official FDA recall classifications for food, drugs, devices, biologics, and tobacco. fda.gov/safety/recalls
- FDA Recalls, Withdrawals & Safety Alerts API - openFDA recall endpoint. open.fda.gov
- USDA Food Safety and Inspection Service (FSIS) - meat, poultry, and processed-egg-product recalls. fsis.usda.gov/recalls
- CDC Foodborne Outbreaks - outbreak investigation context for food recalls. cdc.gov/foodsafety/outbreaks
- Consumer Product Safety Commission (CPSC) - non-food consumer-product recalls cross-reference. cpsc.gov/recalls
- NHTSA Vehicle Recalls - automobile and tire recalls cross-reference. nhtsa.gov/recalls