FDA Recalls, Food, Drug & Medical Device Alerts - Page 13 of 46
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 601–650 of 2,262 FDA recalls. Browse by month →
FDA Recalls
Joy Saffron Cardamon Lassi Recall Issued by Joy Gourmet Foods LLC
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FDA Recalls
Motor City Pizza Co. 5 Cheese Bread Recall
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FDA Recalls high
Zapp's Bayou Blackened Ranch Kettle Chips Recall
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FDA Recalls high
Utz Dirty Sour Cream and Onion Potato Chips Recall
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FDA Recalls
Boichik Bagels Pumpernickel Mix Bagels Recall for Undeclared Sesame
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FDA Recalls high
Dirty Brand Salt and Vinegar Potato Chips Recall
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FDA Recalls high
Prime Food Processing LLC Recalls Dried Herring Fish
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FDA Recalls
Joy Pineapple Lassi Recall Issued for Inadequate Pasteurization
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FDA Recalls high
BD ChloraPrep FREPP Clear Recall Issued by FDA
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FDA Recalls
Sensipar Tablets Recall Due to CGMP Deviations
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FDA Recalls
Sensipar Tablets Recall Due to CGMP Deviations
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FDA Recalls
Sun Pharmaceutical Recalls Perampanel 6mg Tablets
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FDA Recalls
Hydroxyzine Hydrochloride Oral Solution Recall by ANI Pharmaceuticals
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FDA Recalls high
BD ChloraPrep Clear Applicators Recall Issued for Non-Sterility
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FDA Recalls
PReye Vitamin See Eye Drops Recall Issued
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FDA Recalls
Major Methylergonovine Maleate Tablets Recall
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FDA Recalls
Central Admixture Pharmacy Services Recalls Pediatric TPN Bag
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FDA Recalls
BD ChloraPrep FREPP Clear Recall Due to Sterility Issue
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FDA Recalls
Direct Rx Duloxetine Recall for N-Nitroso Impurity
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FDA Recalls
Povi-One Oral Antiseptic Recall Due to Sub Potency
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FDA Recalls
Sensipar Tablets Recall Issued for CGMP Deviations
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FDA Recalls
Fenofibrate Capsules Recall Due to CGMP Deviations
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FDA Recalls
BD ChloraPrep Clear Recall Due to Sterility Concerns
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FDA Recalls
Amgen Recalls Corlanor Tablets Over Foreign Substance
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FDA Recalls
Corlanor Tablets Recalled for Foreign Substance
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FDA Recalls
Lacosamide Tablets Recall Due to Foreign Tablet Mix-Up
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FDA Recalls
Steris HarmonyAIR A-Series Surgical Lighting System Recall
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FDA Recalls high
Arrow International Recalls Drainage and Thoracentesis Kits
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FDA Recalls high
Abiomed Automated Impella Controller Recall
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FDA Recalls high
Arrow International Recalls PSI and MAC Kits
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FDA Recalls
Medline Medical Procedure Kits Recall
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FDA Recalls
Medline Medical Procedure Kits Recall
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FDA Recalls
Medline Industries Recalls Medical Procedure Kits Due to Catheter Issues
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FDA Recalls
ConMed AirSeal Access Port Recall Issued for Overpressure Alerts
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FDA Recalls
Medline Pre-connected Urethral Catheterization Tray Recall
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FDA Recalls
BD Connecta BD Luer-Lok 360 Stopcock Recall
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FDA Recalls
Medline Convenience Kits Recall Due to Adhesive Tubing Issue
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FDA Recalls
Medline Urethral Catheterization Tray Recall Issued
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FDA Recalls high
Arrow International Recalls Arterial Line Kits and RA Cath Kits
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FDA Recalls
Medline Convenience Kits Recall
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FDA Recalls
Medline Urethral Catheterization Tray Recall
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FDA Recalls
STAAR ICL Calculation Software Recall
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FDA Recalls high
Arrow International Recalls CVC Kits
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FDA Recalls
Triathlon Universal Baseplate Size 4 Recall Issued
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FDA Recalls
Medline Convenience Kits Recall
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FDA Recalls
Medline Urethral Catheters Recall Issued
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FDA Recalls high
Datex-Ohmeda Panda Freestanding Warmer Recall
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FDA Recalls
Medline Convenience Kits Recall Due to Adhesive Tubing Issue
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FDA Recalls
Medline HYSTERECTOMY PACK-LF Kits Recall
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FDA Recalls high
Arrow International Kits Recall
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