Product Recalls in California
Product recalls affecting California — including food, drugs, consumer products, medical devices, and vehicles distributed to California. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,064 recalls have been distributed to California in the last 12 months.
Showing 38361–38380 of 56,506 recalls
Recalled Item: Hologic InPlex CF Molecular Test (IVD) Recalled by Hologic, Inc Due to...
The Issue: Complaints of false positive HET mutations and leaking cards; could lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Surgical Americot Blue 3/8" x 2" : 20-26S Recalled by American...
The Issue: Product packaging defective compromising sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Surgical Americot Blue 1/2" x 1/2" : 20-04S Recalled by American...
The Issue: Product packaging defective compromising sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Surgical Ultracot 70 mm x 10090 mm : Recalled by American Surgical...
The Issue: Product packaging defective compromising sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Surgical Ray-Cot 1/2" x 3" : 60-09 Product Recalled by American...
The Issue: Product packaging defective compromising sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Surgical Ultracot 15 mm x 15 mm (Glassine) by American Surgical...
The Issue: Product packaging defective compromising sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Surgical Policot 1/2" x 1/2" : 90-06 Product Recalled by American...
The Issue: Product packaging defective compromising sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Surgical Cotton Balls-Strung 1/2" : 30-02 Product Usage: Recalled...
The Issue: Product packaging defective compromising sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ellipse ICD (Implantable Cardioverter Defibrillator) Model CD2411-36Q...
The Issue: St. Jude Medical is recalling the Ellipse ICD (Implantable Cardioverter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mach 4 Mouse Probe vial within the Mach 4 Universal HRP-Polymer Kit Recalled...
The Issue: Biocare Medical has identified a single lot (082715) of its Mach 4 HRP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mass Eye & Ear Finger Cot Nasal 2's : Recalled by American Surgical Company...
The Issue: Product packaging defective compromising sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Surgical Tonsil Sponges 1" Large : 50-01 Product Recalled by...
The Issue: Product packaging defective compromising sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Surgical Uniqcot 1/2" x 3" : 67-09 Product Recalled by American...
The Issue: Product packaging defective compromising sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dr. Pepper Cherry Recalled by The Coca-Cola Company Due to Undeclared High
The Issue: The product contains undeclared High-fructose Corn Syrup (HFCS).
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ALFALFA SEED Recalled by International Sprout Holding Inc. Due to Potential...
The Issue: One sample taken were positive for Salmonella Poly B
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Fenofibrate Capsules (Micronized) Recalled by Amerisource Health Services...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fenofibrate Capsules (Micronized) Recalled by Amerisource Health Services...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ¿Topicort (desoximetasone) Cream USP Recalled by Taro Pharmaceuticals...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LGD-Xtreme (ligandrol LGD-4033) Recalled by Invisiblu International LLC Due...
The Issue: Marketed Without An Approved NDA/ANDA: Contains an unapproved drug,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: E.cam or Symbia systems that use foresight detectors - Product Recalled by...
The Issue: E. CAM and Symbia system with foresight detectors performing gated or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.