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. 2,899 recalls have been distributed to Florida in the last 12 months.
Showing 9361–9380 of 55,837 recalls
Recalled Item: VITROS Immunodiagnostic Products Troponin I ES Calibrators Recalled by...
The Issue: Reagent packs could potentially contain incorrect wells, which will generate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP) Recalled by Datascope...
The Issue: IABP may lose the ability to charge batteries in one or both bay slots....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cios Select VA 21 with FD- A Mobile X-ray system Recalled by Siemens Medical...
The Issue: Incorrect glue was applied on the plexiglass sheet on the single tank cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Rescue Intra-Aortic Balloon Pump (IABP) Recalled by Datascope...
The Issue: IABP may lose the ability to charge batteries in one or both bay slots....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP) Recalled by Datascope...
The Issue: An unexpected shutdown of the IABP may occur due to failures of tantalum...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Rescue Intra-Aortic Balloon Pump (IABP) Recalled by Datascope...
The Issue: An unexpected shutdown of the IABP may occur due to failures of tantalum...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Design Options¿ / Epidural anesthesia kit (10 count carton) Recalled by B....
The Issue: Kits were assembled with the incorrect Filter Straw.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Exactech Ergo Impactor Handle Recalled by Exactech, Inc. Due to The ball and...
The Issue: The ball and spring housed within the locking mechanism of the handle can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERIGENE Clostridium difficile Nucleic Acid Test Recalled by Luminex...
The Issue: It is possible that in rare instances the VERIGENE CDF Nucleic Acid Test Kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Verigene Enteric Pathogens Nucleic Acid Test (EP) Recalled by Luminex...
The Issue: It is possible that in rare instances the VERIGENE CDF Nucleic Acid Test Kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perifix¿ / Epidural anesthesia kit (10 count carton) Recalled by B. Braun...
The Issue: Kits were assembled with the incorrect Filter Straw.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Exactech Shoulder GPS Impactor Handle Recalled by Exactech, Inc. Due to The...
The Issue: The ball and spring housed within the locking mechanism of the handle can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Cytosponge Cell Collection Device Recalled by Covidien, LLC Due to...
The Issue: Cell Collection Device may be at increased risk of the sponge detaching from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beckman Coulter DxA Automation System Recalled by Beckman Coulter Biomedical...
The Issue: A software defect in the DxA Automation System may cause tests to be run on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beckman Coulter DxA Automation System Recalled by Beckman Coulter Biomedical...
The Issue: A software defect in the DxA Automation System may cause tests to be run on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Everest Garam Masala Recalled by Amin Trading Agency LLC Due to Potential...
The Issue: Product may be contaminated with Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Everest Sambhar Masala Recalled by Amin Trading Agency LLC Due to Potential...
The Issue: Product may be contaminated with Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Maggi Masala ae Magic Recalled by Amin Trading Agency LLC Due to Potential...
The Issue: Product may be contaminated with Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Julian's Recipe Maple & Brown Butter Cauli-Wafels Recalled by Julian's...
The Issue: Contains undeclared soy lecithin
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Julian's Recipe Original Cauli-Wafels Recalled by Julian's Recipe, LLC Due...
The Issue: Contains undeclared soy lecithin
Recommended Action: Do not consume. Return to store for a refund or discard.