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. 2,926 recalls have been distributed to California in the last 12 months.
Showing 17521–17540 of 30,923 recalls
Recalled Item: Edwards Lifesciences Aortic Perfusion Cannula Recalled by SPS Sterilization,...
The Issue: The expiration date on the device labeling exceeds its actual validated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Wallstent Endoprosthesis Tracheobronchial Transhepatic...
The Issue: The expiration date on the device labeling exceeds its actual validated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Wallstent Enteral Endoprosthesis Colonic/Duodenal Stent...
The Issue: The expiration date on the device labeling exceeds its actual validated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Wallstent Endoprosthesis Tracheobronchial Self-Expanding...
The Issue: The expiration date on the device labeling exceeds its actual validated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Wallstent RP Endoprosthesis Tracheobronchial Transhepatic...
The Issue: The expiration date on the device labeling exceeds its actual validated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vascular Solutions Venture Rx Catheter Recalled by SPS Sterilization, Inc...
The Issue: The expiration date on the device labeling exceeds its actual validated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Wallstent RP Endoprosthesis Tracheobronchial...
The Issue: The expiration date on the device labeling exceeds its actual validated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Wallstent Endoprosthesis Tracheobronchial Self-Expanding...
The Issue: The expiration date on the device labeling exceeds its actual validated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences Optisite Arterial Perfusion Cannula Recalled by SPS...
The Issue: The expiration date on the device labeling exceeds its actual validated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences Femoral Venous Cannula Recalled by SPS Sterilization,...
The Issue: The expiration date on the device labeling exceeds its actual validated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci X Surgical System Recalled by Intuitive Surgical, Inc. Due to...
The Issue: Specific da Vinci X Surgical Systems (IS4200) were shipped with defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Evicel Accessory Device - 45 cm Flexible Tip (SET OF 3) Recalled by Ethicon,...
The Issue: Products labeled for distribution outside the United States may have been...
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: Part no. 690.380 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: Part no. 690.375 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: ST-AIA PACK Testosterone Recalled by Tosoh Bioscience Inc Due to Asfotase...
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 Cort 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 Prolactin 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 FSH 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 CA 19-9 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.