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 2664126660 of 30,686 recalls

Medical DeviceMarch 5, 2014· Mevion Medical Systems, Inc.

Recalled Item: MEVION S250 Recalled by Mevion Medical Systems, Inc. Due to Geometric...

The Issue: Geometric positioning error can occur after a rotational correction has been...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2014· Pega Medical Inc.

Recalled Item: Fassier-Duval IM Telescopic System. Orthopedic intramedullary rod implant....

The Issue: The outer package label contained the incorrect length of the device. There...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2014· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: DPM 6 Monitor in use with a Multi Parameter Module Recalled by Mindray DS...

The Issue: The MPM included a cardiac ST/Arrhythmia analysis feature which is not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2014· Alfa Wassermann, Inc.

Recalled Item: Alfa Wassermann Diagnostic Technologies Recalled by Alfa Wassermann, Inc....

The Issue: Extremely low absorbance readings.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2014· LumiQuick Diagnostics Inc.

Recalled Item: Syphilis Test Card Whole Blood(Serum) LumiQuick Recalled by LumiQuick...

The Issue: Products shipped to US locations that do not have approved applications for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2014· LumiQuick Diagnostics Inc.

Recalled Item: Propoxyphene Test Strip Recalled by LumiQuick Diagnostics Inc. Due to...

The Issue: Products shipped to US locations that do not have approved applications for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2014· LumiQuick Diagnostics Inc.

Recalled Item: Myoglobin Test Card (Serum) Recalled by LumiQuick Diagnostics Inc. Due to...

The Issue: Products shipped to US locations that do not have approved applications for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2014· LumiQuick Diagnostics Inc.

Recalled Item: Cocaine Strip Recalled by LumiQuick Diagnostics Inc. Due to Products shipped...

The Issue: Products shipped to US locations that do not have approved applications for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2014· Thoratec Corporation

Recalled Item: HeartMate II LVAD Pump and Pock Controller Kit Recalled by Thoratec...

The Issue: Discovery of serious injuries and deaths associated with the process of...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 4, 2014· LumiQuick Diagnostics Inc.

Recalled Item: Barbiturate Strip Recalled by LumiQuick Diagnostics Inc. Due to Products...

The Issue: Products shipped to US locations that do not have approved applications for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2014· Thoratec Corporation

Recalled Item: HeartMate II System Controller Product Usage: HeartMate II is a Recalled by...

The Issue: Discovery of serious injuries and deaths associated with the process of...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 4, 2014· LumiQuick Diagnostics Inc.

Recalled Item: CK-MB Test Card (Whole Blood) Recalled by LumiQuick Diagnostics Inc. Due to...

The Issue: Products shipped to US locations that do not have approved applications for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2014· LumiQuick Diagnostics Inc.

Recalled Item: MDMA/Ecstasy Test Card Recalled by LumiQuick Diagnostics Inc. Due to...

The Issue: Products shipped to US locations that do not have approved applications for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2014· LumiQuick Diagnostics Inc.

Recalled Item: Clonazepam Test Card Recalled by LumiQuick Diagnostics Inc. Due to Products...

The Issue: Products shipped to US locations that do not have approved applications for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2014· LumiQuick Diagnostics Inc.

Recalled Item: Oxycodone Strip Recalled by LumiQuick Diagnostics Inc. Due to Products...

The Issue: Products shipped to US locations that do not have approved applications for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2014· LumiQuick Diagnostics Inc.

Recalled Item: Tramadol Strip Recalled by LumiQuick Diagnostics Inc. Due to Products...

The Issue: Products shipped to US locations that do not have approved applications for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2014· LumiQuick Diagnostics Inc.

Recalled Item: EDDP Test Card Recalled by LumiQuick Diagnostics Inc. Due to Products...

The Issue: Products shipped to US locations that do not have approved applications for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2014· LumiQuick Diagnostics Inc.

Recalled Item: Salmonella typhi Antigen Test Card Recalled by LumiQuick Diagnostics Inc....

The Issue: Products shipped to US locations that do not have approved applications for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2014· LumiQuick Diagnostics Inc.

Recalled Item: Amphetamine Strip Recalled by LumiQuick Diagnostics Inc. Due to Products...

The Issue: Products shipped to US locations that do not have approved applications for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2014· LumiQuick Diagnostics Inc.

Recalled Item: Malaria pf Antigen Test Card Recalled by LumiQuick Diagnostics Inc. Due to...

The Issue: Products shipped to US locations that do not have approved applications for...

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

Class II — Potential Health HazardOngoing