FDA Recalls, Food, Drug & Medical Device Alerts - Page 17 of 27
Latest food, drug, and medical device recalls issued by the U.S. Food and Drug Administration. Class I, II, and III recall classifications, affected products, and consumer guidance.
Showing 801–850 of 1,348 FDA recalls. Browse by month →
FDA Recalls
FDA Recall of eTRAX Needle System Starter Kit
FDA ·
FDA Recalls high
Recall of Medtronic MiniMed 720G Insulin Pump
FDA ·
FDA Recalls
Recall of da Vinci S, Si Permanent Cautery Hook Instrument
FDA ·
FDA Recalls
GE Healthcare LLC Announces Recall of SIGNA Premier Systems
FDA ·
FDA Recalls high
Recall of THORACIC ROBOTS DYNJ908777B by Medline Industries
FDA ·
FDA Recalls
FDA Recall of MEI HEONG YUEN Garlic Flavor Roasted Peanuts
FDA ·
FDA Recalls
FDA Recall of MEI HEONG YUEN Walnut Flavor Roasted Peanuts Due to Banned Sweetener
FDA ·
FDA Recalls
FDA Announces Recall of Imu-Tek Colostrum-5 Powder
FDA ·
FDA Recalls
FDA Announces Recall of Divided Sunset Multi Collagen Peptides
FDA ·
FDA Recalls
HEYTEA USA Inc. Recalls Coconut Drink 1 Over Undeclared Milk
FDA ·
FDA Recalls
Recall of MEI HEONG YUEN Tangerine Flavor Roasted Peanuts
FDA ·
FDA Recalls
FDA Recall of Imu-Tek Colostrum-5 Capsules Announced
FDA ·
FDA Recalls
FDA Recall of Mama Rose's Prickly Pear Salad Dressing Due to Undeclared Sulfites
FDA ·
FDA Recalls
FDA Recall of Pocas International's Popping Boba RTD Peach Oolong Tea
FDA ·
FDA Recalls
Recall of POPPING BOBA RTD MANGO PASSION FRUIT GREEN TEA
FDA ·
FDA Recalls
Recall of POPPING BOBA RTD STRAWBERRY DRAGON F/OOLONG TEA
FDA ·
FDA Recalls
FDA Recall of JFE Franchising Dumpling Products Due to Glass Contamination
FDA ·
FDA Recalls
Recall of POPPING BOBA RTD MIXED BERRY HIBISCUS TEA by Pocas International Corp.
FDA ·
FDA Recalls
Recall of Dumpling Vegetable Products by JFE Franchising Inc.
FDA ·
FDA Recalls high
FDA Recall of Lone Star Dairy Products' Spray Dried Dairy Powder Due to Salmonella
FDA ·
FDA Recalls
Prickly Pear Jelly Recall by The Maros Group Due to Undeclared Milk
FDA ·
FDA Recalls
Recall of Sterile Eye Drops by K.C. Pharmaceuticals Due to Sterility Concerns
FDA ·
FDA Recalls
Recall of Various Eye Drops Due to Sterility Concerns
FDA ·
FDA Recalls
FDA Recall of Various Eye Drop Brands Over Sterility Concerns
FDA ·
FDA Recalls
FDA Recall of Prazosin Hydrochloride Capsules by Biocon Pharma
FDA ·
FDA Recalls high
Recall of Magnesium Sulfate in Water for Injection by Amneal Pharmaceuticals
FDA ·
FDA Recalls high
Recall of Various Eye Drop Brands Due to Sterility Concerns
FDA ·
FDA Recalls
Recall of Artificial Tears and Other Eye Drops Announced
FDA ·
FDA Recalls
Recall of Multiple Eye Drop Brands Due to Sterility Concerns
FDA ·
FDA Recalls
FDA Announces Recall of Ultra Lubricating Eye Drops
FDA ·
FDA Recalls
Recall of Artificial Tears Eye Drops Due to Sterility Concerns
FDA ·
FDA Recalls
FDA Announces Recall of Prazosin Hydrochloride Capsules
FDA ·
FDA Recalls
FDA Recalls Tramadol Hydrochloride Tablets Over Impurity Issue
FDA ·
FDA Recalls
Recall of Prazosin Hydrochloride Capsules Due to Impurity Concerns
FDA ·
FDA Recalls high
Recall of Philips Respironics Trilogy Evo Ventilator
FDA ·
FDA Recalls high
Recall of Puracol and Puracol Plus Collagen Wound Dressings
FDA ·
FDA Recalls
FDA Recall of Pelvic Reconstruction System by I.T.S. GmbH
FDA ·
FDA Recalls
Recall of Philips L12-5 Ultrasound Transducer
FDA ·
FDA Recalls
Recall of Olympus HALO PKS Cutting Forceps Due to Welding Defect
FDA ·
FDA Recalls
FDA Recall of MicroScan Neg MIC 56 Due to Contamination
FDA ·
FDA Recalls high
FDA Recall of Volar Radius Plate by I.T.S. GmbH
FDA ·
FDA Recalls high
FDA Class I Recall for Erbe USA Inc's Flexible Cryoprobe
FDA ·
FDA Recalls
FDA Recall for Philips C9-4 Ultrasound Transducer
FDA ·
FDA Recalls
BiDop 3 Pocket Doppler Recall Issued by FDA
FDA ·
FDA Recalls
FDA Recall of Olympus PKS Cutting Forceps Due to Welding Defect
FDA ·
FDA Recalls
Recall of Olympus Everest Bipolar Cutting Forceps
FDA ·
FDA Recalls
Recall of I.T.S. GmbH Pilon Plates Over MRI Safety Concerns
FDA ·
FDA Recalls
FDA Recall of Philips X7-2 Ultrasound Transducer
FDA ·
FDA Recalls
Recall of Philips 3D6-2 Ultrasound Transducer
FDA ·
FDA Recalls high
Recall of FR.O.H. Calcaneus Repair System Due to MRI Safety Concerns
FDA ·