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. 2,940 recalls have been distributed to Florida in the last 12 months.
Showing 1281–1300 of 30,686 recalls
Recalled Item: Battery Operated infusion pumps. t:slim X2 G5 Recalled by Tandem Diabetes...
The Issue: Insulin pumps manufactured with speakers from Revision A and B may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STA-Liquid Anti-Xa 4. Model/Catalog Number: 00311US. The STA - Liquid...
The Issue: Potential for contamination of STA-LIQUID ANTI-Xa by Stago Fibrinogen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STA Satellite. Product Code: All . All software versions. The Recalled by...
The Issue: Potential for contamination of STA-LIQUID ANTI-Xa by Stago Fibrinogen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STA-Liquid Anti-Xa 8. Model/Catalog Number: 00322US. The STA - Liquid...
The Issue: Potential for contamination of STA-LIQUID ANTI-Xa by Stago Fibrinogen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STA - Fibrinogen 5. Model/Catalog Number: 00674. The STA - Recalled by...
The Issue: Potential for contamination of STA-LIQUID ANTI-Xa by Stago Fibrinogen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Ultra IABP Catheter Kit Product Name: Ultra IABP Recalled by...
The Issue: Device contains indications for use and device compatibility claims that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: DJO SURGICAL Product Name: ALTIVATE REVERSE WEDGE GLENOID...
The Issue: Their is a potential that the reamer may kick or bind up during or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: DJO SURGICAL Product Name: FA S Altivate Reverse Recalled by...
The Issue: Their is a potential that the reamer may kick or bind up during or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: DJO SURGICAL Product Name: ALTIVATE REVERSE WEDGE GLENOID...
The Issue: Their is a potential that the reamer may kick or bind up during or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: DJO SURGICAL Product Name: ALTIVATE REVERSE WEDGE GLENOID...
The Issue: Their is a potential that the reamer may kick or bind up during or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureStep Foley Tray System Bardex I.C. Complete Care Infection Control...
The Issue: Foley catheter trays have incorrect inserts, user may think:1)Silicone, when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureStep Foley Tray System Lubri-Sil I.C. Complete Care Infection Control...
The Issue: Foley catheter trays have incorrect inserts, user may think:1)Silicone, when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureStep Foley Tray System BARD¿ Lubri-Sil Foley Catheter Tray Recalled by...
The Issue: Foley catheter trays have incorrect inserts, user may think:1)Silicone, when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ReQuest Measles IgM Product Name: Enzyme Linked Immunoabsorbant...
The Issue: Measles IgM Test Kit lacks premarket approval or clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orthopedic Pack Recalled by O&M HALYARD INC Due to Surgical drape packs may...
The Issue: Surgical drape packs may have open seals, which may compromise the sterility...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IPC Powerease System UDI-DI: 00613994448705 00643169406834. The IPC Recalled...
The Issue: Due to out of the box wobble of the driver.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pinnacle 3 with TumorLOC Recalled by Philips Medical Systems (Cleveland) Inc...
The Issue: Due to software issue, Radiation Therapy Planning system may provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TOPS Inserter Recalled by PREMIA SPINE LTD Due to Potential for missing pins...
The Issue: Potential for missing pins at tip of inserter.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pentax Medical Video Processor Recalled by Pentax of America Inc Due to...
The Issue: During endoscopic procedures using a combination of the video processor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dynex Agility Sample Tips Recalled by Dynex Technologies, Inc. Due to The...
The Issue: The internal label affixed to the sample tip rack is incorrectly labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.