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.

55,837 total recalls
2,710 in last 12 months

Showing 2496124980 of 30,686 recalls

Medical DeviceNovember 21, 2014· Smiths Medical ASD, Inc.

Recalled Item: Hypodermic Needle Pro¿ Edge" Safety Device with Syringe 20G x1 Recalled by...

The Issue: Needle is not captured in the needle safety sheath in specific lots.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2014· Smiths Medical ASD, Inc.

Recalled Item: Hypodermic Needle Pro¿ Edge" Safety Device 20G x1 Recalled by Smiths Medical...

The Issue: Needle is not captured in the needle safety sheath in specific lots.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2014· Atricure Inc

Recalled Item: Cryogenic probe for cardiac ablation surgery Recalled by Atricure Inc Due to...

The Issue: Affected product may have compromised sterility due to packaging defects. It...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2014· Teleflex, Inc.

Recalled Item: Bronchial Double Lumen Tube Set (Left) Recalled by Teleflex, Inc. Due to...

The Issue: Customer complaints reporting that the cobb connector detached from the main...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHEK Tender II 17/80 10 + 10 pieces Product Usage: Recalled by Roche...

The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHEK Tender I 17/80 10 pieces Product Usage: Intended for Recalled by...

The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHEK Tender I 17/110 10 pieces Product Usage: Intended for Recalled by...

The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2014· Philips Medical Systems, Inc.

Recalled Item: Lithium Polymer Fiber Optic Module Batteries used in the Intera Recalled by...

The Issue: VCG battery ignited in a VCG unit when recharging.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2014· Phadia US Inc

Recalled Item: Phadia 1000 Instrument (introduced as UniCAP 1000) Recalled by Phadia US Inc...

The Issue: During an investigation of instrument logs it was determined that In...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHEK Tender II 13/80 10 + 10 pieces Product Usage: Recalled by Roche...

The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2014· Unistrip Technologies LLC

Recalled Item: UniStrip1 Recalled by Unistrip Technologies LLC Due to Failure to submit a...

The Issue: Failure to submit a 510(k) for device labeling changes.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHEK¿ Tender I 13/60 10 pieces Product Usage: Usage: Intended Recalled...

The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHEK Tender I 17/60 10 pieces Product Usage: Intended for Recalled by...

The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHEK Tender II 13/60 10 + 10 pieces Product Usage: Recalled by Roche...

The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHEK Tender I 13/110 10 pieces Product Usage: Intended for Recalled by...

The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHEK Tender I 13/80 10 pieces Product Usage: Intended for Recalled by...

The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHEK Tender II 17/60 10 + 10 pieces Product Usage: Recalled by Roche...

The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHEK Tender II 17/110 10 + 10 pieces Product Usage: Recalled by Roche...

The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHEK Tender II 13/110 10 + 10 pieces Product Usage: Recalled by Roche...

The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2014· Philips Medical Systems, Inc.

Recalled Item: Philips HeartStart MRx Monitor/Defibrillator Models:M3535A Recalled by...

The Issue: MRx Defib can be susceptible to one or both issues: 1. The C02 Inlet Port...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing