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. 2,839 recalls have been distributed to California in the last 12 months.
Showing 29481–29500 of 56,506 recalls
Recalled Item: ST-AIA PACK IRI Recalled by Tosoh Bioscience Inc Due to Asfotase Alfa...
The Issue: Asfotase Alfa (Strensiq) interferes with certain Tosoh assays which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ST-AIA PACK TT3 Recalled by Tosoh Bioscience Inc Due to Asfotase Alfa...
The Issue: Asfotase Alfa (Strensiq) interferes with certain Tosoh assays which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Part no. 690.379 Recalled by Synthes (USA) Products LLC Due to Affected...
The Issue: Affected screw gauges incorrectly measure screws 5.41mm shorter than the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD MAX DNA MMK (SPC) For Laboratory Use Recalled by Becton Dickinson & Co....
The Issue: The package insert incorrectly lists the volume of the primer and probe...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Getinge AGS Recalled by Getinge Disinfection Ab Due to There is potential...
The Issue: There is potential for a cart with disinfected goods to unload without the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Getinge AGS Recalled by Getinge Disinfection Ab Due to There is potential...
The Issue: There is potential for a cart with disinfected goods to unload without the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD MAX DNA MMK Lab Use Recalled by Becton Dickinson & Co. Due to The package...
The Issue: The package insert incorrectly lists the volume of the primer and probe...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lipase Recalled by Randox Laboratories Ltd. Due to Randox has now released...
The Issue: Randox has now released further steps to avoid contamination of the Lipase...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BECKMAN COULTER iChemVELOCITY Recalled by Beckman Coulter Inc. Due to...
The Issue: Beckman Coulter has determined that there is a potential for incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flucanazole Injection Recalled by Renaissance Lakewood, LLC Due to...
The Issue: Superpotent and Failed Stability Specifications; out of specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Food Club Recalled by Gilster-Mary Lee Corp. Due to Undeclared Wheat
The Issue: Puffed wheat cereal was packaged using puffed rice packaging, resulting in...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: XZB Grilled Crispy Shrimp (20g*20 and 16g*24) Code (16g) 6923006800082...
The Issue: Product tested positive for nitrofurans.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Fabius GS Premium Recalled by Draeger Medical, Inc. Due to The automatic...
The Issue: The automatic ventilation may fail if the position detection of the motor is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fabius MRI Recalled by Draeger Medical, Inc. Due to The automatic...
The Issue: The automatic ventilation may fail if the position detection of the motor is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer M/L Taper Hip Prosthesis Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Certain packages labeled as size 7.5 Extended Offset Reduced Neck length hip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fabius Tiro M Recalled by Draeger Medical, Inc. Due to The automatic...
The Issue: The automatic ventilation may fail if the position detection of the motor is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer M/L Taper Hip Prosthesis Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Certain packages labeled as size 7.5 Extended Offset Reduced Neck length hip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fabius Tiro Recalled by Draeger Medical, Inc. Due to The automatic...
The Issue: The automatic ventilation may fail if the position detection of the motor is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIDAS LH Recalled by bioMerieux, Inc. Due to Several complaints were...
The Issue: Several complaints were received for invalid calibration with low calibrator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Biomet Comprehensive Segmental Revision System (SRS). Orthopedic...
The Issue: During assembly, an SRS Humeral Distal Body implant failed to engage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.