Product Recalls in Florida
Product recalls affecting Florida — including food, drugs, consumer products, medical devices, and vehicles distributed to Florida. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,615 recalls have been distributed to Florida in the last 12 months.
Showing 53461–53480 of 55,837 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: 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: Frozen Publix Brand Premium Tempura Shrimp Recalled by Publix Corporate...
The Issue: On 10/16/2012, Publix Super Markets, Inc. recalled their Publix Premium...
Recommended Action: Do not consume. Return to store for a refund or discard.
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.