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. 2,654 recalls have been distributed to California in the last 12 months.
Showing 54021–54040 of 56,506 recalls
Recalled Item: PureFit Peanut Butter Bars Recalled by PureFit Inc Due to Potential...
The Issue: PureFit is recalling PureFit Peanut Butter Crunch Bars because of possible...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling
The Issue: The product may mislabel patient information on culture specimen bottles due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling
The Issue: The product may mislabel patient information on culture specimen bottles due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling
The Issue: The product may mislabel patient information on culture specimen bottles due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling
The Issue: The product may mislabel patient information on culture specimen bottles due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling
The Issue: The product may mislabel patient information on culture specimen bottles due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling
The Issue: The product may mislabel patient information on culture specimen bottles due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling
The Issue: The product may mislabel patient information on culture specimen bottles due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling
The Issue: The product may mislabel patient information on culture specimen bottles due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling
The Issue: The product may mislabel patient information on culture specimen bottles due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Corometrics Qwik Connect Plus Spiral Electrode- Model #7000AA0 A fetal...
The Issue: Thirty fetal scalp electrodes were found to have an incomplete package seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling
The Issue: The product may mislabel patient information on culture specimen bottles due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling
The Issue: The product may mislabel patient information on culture specimen bottles due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling
The Issue: The product may mislabel patient information on culture specimen bottles due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux BacT/ALERT Combo Module Recalled by Biomerieux Inc Due to Mislabeling
The Issue: The product may mislabel patient information on culture specimen bottles due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux BacT/ALERT Control Module Recalled by Biomerieux Inc Due to...
The Issue: The product may mislabel patient information on culture specimen bottles due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux BacT/ALERT Combo Module Recalled by Biomerieux Inc Due to Mislabeling
The Issue: The product may mislabel patient information on culture specimen bottles due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling
The Issue: The product may mislabel patient information on culture specimen bottles due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling
The Issue: The product may mislabel patient information on culture specimen bottles due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling
The Issue: The product may mislabel patient information on culture specimen bottles due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.