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 1481–1500 of 30,686 recalls
Recalled Item: Automated Impella Controller (AIC) Recalled by Abiomed, Inc. Due to A...
The Issue: A potential issue with the Automated Impella Controller (AIC) not detecting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD COR System Software. Model Number: 444829. Recalled by Becton Dickinson &...
The Issue: Potential for functionality issue that supports the Over labeling feature...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: HeartMate Product Name: Mobile Power Unit Recalled by Thoratec...
The Issue: Due to misaligned V-Lock feature on the Mobile Power Unit power cords, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Nellcor Bedside SpO2 Patient Monitoring System: Recalled by...
The Issue: Bedside SpO2 Patient Monitoring System alarms not heard/recognized,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: HeartMate Product Name: Mobile Power Unit Model/Catalog Number:...
The Issue: Due to misaligned V-Lock feature on the Mobile Power Unit power cords, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter SIGMA Spectrum Infusion Pump V8 Recalled by Baxter Healthcare...
The Issue: Certain Spectrum infusion pumps may have an incorrect version of software.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: One-piece Guedel airway Recalled by Intersurgical Inc Due to Potential...
The Issue: Potential contamination with small burrs, which if detach could be inhaled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinia Recalled by GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING Due to...
The Issue: Unintended radial detector motion may occur during patient setup or during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: One-piece Guedel airway Recalled by Intersurgical Inc Due to Potential...
The Issue: Potential contamination with small burrs, which if detach could be inhaled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter SIGMA Spectrum Infusion Pump V6 Recalled by Baxter Healthcare...
The Issue: Certain Spectrum infusion pumps may have an incorrect version of software.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Varicam Recalled by GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING Due to...
The Issue: Unintended radial detector motion may occur during patient setup or during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Osteotec Product Name: Osteotec Silicone Finger Implant...
The Issue: There is the potential that the silicone implant may contain foreign material
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Recalled by Stryker Corporation Due to Due to complaints their is...
The Issue: Due to complaints their is the potential that irrigation solution may leaked...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic CareLink SmartSync Device Manager Recalled by Medtronic, Inc. Due...
The Issue: In prior SmartSync application versions, the Abort button stopped the test...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic CareLink SmartSync Patient Connector Recalled by Medtronic, Inc....
The Issue: In prior SmartSync application versions, the Abort button stopped the test...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bardex Lubri-Sil I.C. 400-series Temperature Sensing Silver/Hydrogel Coated...
The Issue: Foley catheter may have an obstructed lumen, which may result in an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Recalled by Stryker Corporation Due to Due to complaints their is...
The Issue: Due to complaints their is the potential that irrigation solution may leaked...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MI Cancer Seek UDI Code: (01)00860008613325(21)H5HJHDSXF MI Cancer Recalled...
The Issue: Due to an incorrect test results provided that indicated the incorrect drug...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QuickVue: Dipstick Strep A Test: 50T Recalled by Quidel Corporation Due to...
The Issue: Dipstick strep A test has potential for false positive results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: i-view video laryngoscope. Model Number: 8008000. The i-view video...
The Issue: Potential for faulty devices as a result of depleted batteries.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.