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 2566125680 of 30,686 recalls

Medical DeviceAugust 5, 2014· Curbell Medical, Inc.

Recalled Item: CURBELL MEDICAL CareSense Wireless Advanced LCD Bed and Chair Monitor...

The Issue: The firm became aware of a potential problem that was initiated by a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2014· Medical Components, Inc dba MedComp

Recalled Item: Split Cath III Trays Recalled by Medical Components, Inc dba MedComp Due to...

The Issue: The Split Cath III Trays were incorrectly labeled as 16F x 32CM Split Cath...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2014· Sorin Group USA, Inc.

Recalled Item: ST¿CKERT HeaterCooler System 3T Recalled by Sorin Group USA, Inc. Due to On...

The Issue: On August 1, 2014 Sorin Group USA, Inc. informed consignees via letter to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: Roche cobas IT 1000 Product Usage: Intended Use: An electronic Recalled by...

The Issue: Potential that test results would be assigned to the wrong Patient ID if...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2014· Carefusion 2200 Inc

Recalled Item: CareFusion AirLife Heated Infant Breathing Circuit Product Usage:...

The Issue: The CareFusion AirLife Heated Infant Breathing Circuit is being recalled due...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2014· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: Mindray V21 Recalled by Mindray DS USA, Inc. dba Mindray North America Due...

The Issue: Mindray DS USA Inc. initiated a voluntary field corrective action for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2014· Integra York PA, Inc

Recalled Item: Integra Container Lid Recalled by Integra York PA, Inc Due to Integra...

The Issue: Integra LifeSciences has identified through an internal investigation that...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2014· Wright Medical Technology, Inc.

Recalled Item: CLAW II 2 HOLE PLATE ORTHOLOC 3DSi Recalled by Wright Medical Technology,...

The Issue: Plates manufactured from an incorrect raw material.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2014· Wright Medical Technology, Inc.

Recalled Item: CLAW II STRAIGHT PLATE ORTHOLOC 3DSi Recalled by Wright Medical Technology,...

The Issue: Plates manufactured from an incorrect raw material.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2014· Wright Medical Technology, Inc.

Recalled Item: CLAW II STRAIGHT PLATE ORTHOLOC 3DSi Recalled by Wright Medical Technology,...

The Issue: Plates manufactured from an incorrect raw material.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2014· Wright Medical Technology, Inc.

Recalled Item: CLAW PLATE 20mm INTERAXIS CHARLOTTE F&A SYSTEM Recalled by Wright Medical...

The Issue: Plates manufactured from an incorrect raw material.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2014· Wright Medical Technology, Inc.

Recalled Item: CLAW II 2 HOLE PLATE ORTHOLOC 3DSi Recalled by Wright Medical Technology,...

The Issue: Plates manufactured from an incorrect raw material.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2014· Wright Medical Technology, Inc.

Recalled Item: CLAW II STRAIGHT PLATE ORTHOLOC 3DSi Recalled by Wright Medical Technology,...

The Issue: Plates manufactured from an incorrect raw material.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2014· Wright Medical Technology, Inc.

Recalled Item: CLAW II 2 HOLE PLATE ORTHOLOC 3DSi Recalled by Wright Medical Technology,...

The Issue: Plates manufactured from an incorrect raw material.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2014· Wright Medical Technology, Inc.

Recalled Item: CLAW II 2 HOLE PLATE ORTHOLOC 3DSi Recalled by Wright Medical Technology,...

The Issue: Plates manufactured from an incorrect raw material.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2014· Wright Medical Technology, Inc.

Recalled Item: CLAW 3.5mm PLATE CHARLOTTE F&A SYSTEM Recalled by Wright Medical Technology,...

The Issue: Plates manufactured from an incorrect raw material.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2014· Zimmer, Inc.

Recalled Item: Zimmer Gender Solution Patello-Femoral Joint (PFJ) System Patello-Femoral...

The Issue: Internal review found that five (5) PFJ implant forgings were identified as...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2014· Siemens Medical Solutions USA, Inc.

Recalled Item: The Symbia Intevo series consists of the Intevo 16 Recalled by Siemens...

The Issue: Siemens Medical Solutions USA, Inc. is performing a field correction because...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2014· Illumina Inc

Recalled Item: Illumina Worklist Manager (IWM) (software v1.0.15) Recalled by Illumina Inc...

The Issue: A software component of the MiSeqDx instrument, called the Illumina Worklist...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2014· Becton Dickinson & Co.

Recalled Item: BD BBL Vancomycin Screen Agar Catalog number 222204 Vancomycin Screen...

The Issue: These lots of Agar may have exhibited breakthrough growth of vancomycin...

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

Class II — Potential Health HazardOngoing