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. 3,020 recalls have been distributed to California in the last 12 months.
Showing 10281–10300 of 30,923 recalls
Recalled Item: Dragonfly Laryngeal Surface Electrode Recalled by Spes Medica Due to The...
The Issue: The supplier informed them of possible deviations of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SNS Disposable Urethral Catheter Electrode Recalled by Spes Medica Due to...
The Issue: The supplier informed them of possible deviations of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dragonfly Laryngeal Surface Electrode Recalled by Spes Medica Due to The...
The Issue: The supplier informed them of possible deviations of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Angio Pack Recalled by Windstone Medical Packaging, Inc. Due to Angio tubing...
The Issue: Angio tubing included within Custom Convenience kits may contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Angio Pack Recalled by Windstone Medical Packaging, Inc. Due to Angio tubing...
The Issue: Angio tubing included within Custom Convenience kits may contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revogene SARS-CoV-2 Catalog Number: 410700 IVD for real-time Reverse...
The Issue: Emergency Use Application (EUA) application withdrawn as false negative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revogene RNA Software Upgrade Kit Revogene RNA Software Upgrade USBs...
The Issue: Emergency Use Application (EUA) application withdrawn as false negative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CANNU-Flex SILK Interference Screws 6 mmx 30 mm - Product Recalled by Smith...
The Issue: Mislabeled box contained a 6mm x 20mm screw instead of 6mm x 30mm screw
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....
The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....
The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....
The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....
The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....
The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....
The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....
The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....
The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....
The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elecsys Troponin I STAT Immunoassay: Catalog# 05094798160 - Product Usage:...
The Issue: Recall reason is possible sporadic false negative conventional troponin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....
The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....
The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.