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. 2,710 recalls have been distributed to Florida in the last 12 months.
Showing 28001–28020 of 30,686 recalls
Recalled Item: The SurgiCounter Charging Cradle Product Usage: SurgiCounter Charging...
The Issue: Faulty SurgiCounter Charging Cradle can prevent the scanner from charging or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Streamline MIS Spinal Fixation System Fixed Rod Holder NON STERILE Recalled...
The Issue: The affected fixed rod holders did not allow the instrument to lock down on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...
The Issue: A product issue has been identified for customers using software version...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...
The Issue: A product issue has been identified for customers using software version...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...
The Issue: A product issue has been identified for customers using software version...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...
The Issue: A product issue has been identified for customers using software version...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...
The Issue: A product issue has been identified for customers using software version...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...
The Issue: A product issue has been identified for customers using software version...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...
The Issue: A product issue has been identified for customers using software version...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...
The Issue: A product issue has been identified for customers using software version...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...
The Issue: A product issue has been identified for customers using software version...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...
The Issue: A product issue has been identified for customers using software version...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...
The Issue: A product issue has been identified for customers using software version...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...
The Issue: A product issue has been identified for customers using software version...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...
The Issue: A product issue has been identified for customers using software version...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...
The Issue: A product issue has been identified for customers using software version...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...
The Issue: A product issue has been identified for customers using software version...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brivo NM615 Recalled by GE Healthcare, LLC Due to GE became aware of an...
The Issue: GE became aware of an incident at a VA Medical Center facility in the US in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery NM 630 Recalled by GE Healthcare, LLC Due to GE became aware of an...
The Issue: GE became aware of an incident at a VA Medical Center facility in the US in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Varicam/VG and VG Hawkeye devices Product Usage: The Recalled...
The Issue: GE became aware of an incident at a VA Medical Center facility in the US in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.