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. 2,939 recalls have been distributed to Florida in the last 12 months.
Showing 1621–1640 of 30,686 recalls
Recalled Item: BD Insyte Autoguard Winged Shielded IV Catheter Recalled by Becton Dickinson...
The Issue: Due to customer complaints, there is the possibility that catheter needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Insyte Autoguard Shielded IV Catheter Recalled by Becton Dickinson...
The Issue: Due to customer complaints, there is the possibility that catheter needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Becton Dickinson Infusion Therapy Systems, Inc. Due to Due to...
The Issue: Due to customer complaints, there is the possibility that catheter needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Becton Dickinson Infusion Therapy Systems, Inc. Due to Due to...
The Issue: Due to customer complaints, there is the possibility that catheter needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Becton Dickinson Infusion Therapy Systems, Inc. Due to Due to...
The Issue: Due to customer complaints, there is the possibility that catheter needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Becton Dickinson Infusion Therapy Systems, Inc. Due to Due to...
The Issue: Due to customer complaints, there is the possibility that catheter needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Becton Dickinson Infusion Therapy Systems, Inc. Due to Due to...
The Issue: Due to customer complaints, there is the possibility that catheter needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bigfoot Unity Diabetes Management System SW-300689-01 Bigfoot Inject v1 Pen...
The Issue: Due to a software/firmware issue diabetes management system may provide a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LUCAS 2 Recalled by Jolife AB Due to Due to demonstration units of chest...
The Issue: Due to demonstration units of chest compression system being provided to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Becton Dickinson Infusion Therapy Systems, Inc. Due to Due to...
The Issue: Due to customer complaints, there is the possibility that catheter needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Newport HT70 Ventilator Recalled by Covidien Due to Ventilator Printed...
The Issue: Ventilator Printed Circuit Board Assembly may have two separate capacitors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: My3D Personalized Solutions Humeral Cup Recalled by Onkos Surgical, Inc. Due...
The Issue: Required inspections were not performed on finished product prior to release...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BACTEC" MGIT" 960 PZA Kit. IVD qualitative procedure for Recalled by...
The Issue: BD has received additional complaints of intermittent false resistance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ColoSense Test Kit Recalled by Geneoscopy, Inc. Due to Multiple plate...
The Issue: Multiple plate failures documented as a result of the Low Positive Template...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRIMA 4MM ECCENTRICAL ADAPTOR WITH SCREW Recalled by Limacorporate S.p.A Due...
The Issue: There is the potential that the eccentrical adaptor with screw, black laser...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRIMA 2MM ECCENTRICAL ADAPTOR WITH SCREW .15.702 Recalled by Limacorporate...
The Issue: There is the potential that the eccentrical adaptor with screw, black laser...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Q-Stop Product Name: Suture Retention Device Model/Catalog...
The Issue: XXX
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline UMBILICAL TRAY W/3.5&5FR CATH Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: There is a possible packaging defect impacting the outer Tyvec pouch that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Broselow Pediatric Emergency Rainbow Tape (distribution by AirLife) Recalled...
The Issue: The impacted tape was manufactured with incorrect information on the tape....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Contamac Recalled by Contamac Solutions, Inc. Due to Contact lens insertion...
The Issue: Contact lens insertion solution may lack sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.