Product Recalls in Rhode Island
Product recalls affecting Rhode Island — including food, drugs, consumer products, medical devices, and vehicles distributed to Rhode Island. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,263 recalls have been distributed to Rhode Island in the last 12 months.
Showing 45861–45880 of 47,970 recalls
Recalled Item: Peanuts in Shell Recalled by Energy Club Inc Due to Potential Salmonella...
The Issue: Trifecta Foods, LLC in Pacoima, CA is voluntarily recalling products...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Peanuts in Shell Recalled by Energy Club Inc Due to Potential Salmonella...
The Issue: Trifecta Foods, LLC in Pacoima, CA is voluntarily recalling products...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 0.9% Sodium Chloride Injections Recalled by Biomerieux Inc Due to The firm...
The Issue: The firm inventoried and distributed 0.9% Sodium Chloride Saline bags as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Green & Black's Organic Peanut & Sea Salt Milk Chocolate Recalled by...
The Issue: Mondelez Global LLC (Mondelez Global) is voluntarily recalling the U.S....
Recommended Action: Do not consume. Return to store for a refund or discard.
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.