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. 2,615 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
2,615 in last 12 months

Showing 5462154640 of 55,837 recalls

Medical DeviceJune 20, 2012· Philips Healthcare Inc.

Recalled Item: Philips HeartStart MRx monitor/defibrillators Models: M3535A Recalled by...

The Issue: HeartStart MRx Unexpected Pads/Paddles ECG Failure

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2012· Eos Imaging Inc

Recalled Item: EOS X-ray Medical Diagnostic Recalled by Eos Imaging Inc Due to It was...

The Issue: It was discovered of several generator failures of the EOS System due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2012· Advanced Sterilization Products

Recalled Item: STERRAD NX Cassette Recalled by Advanced Sterilization Products Due to...

The Issue: Advanced Sterilization Products (ASP) is recalling (removing) the Sterrad...

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

Class III — Low RiskOngoing
Medical DeviceJune 19, 2012· Advanced Sterilization Products

Recalled Item: STERRAD 100S Cassette Recalled by Advanced Sterilization Products Due to...

The Issue: Advanced Sterilization Products (ASP) is recalling (removing) the Sterrad...

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

Class III — Low RiskOngoing
Medical DeviceJune 19, 2012· CareFusion 203, Inc.

Recalled Item: CareFusion EnVe Ventilator Designed for use on patients who require Recalled...

The Issue: CareFusion identified that the EnVe Ventilator may not hold the set Positive...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 19, 2012· Stryker Endoscopy

Recalled Item: Stryker brand Arthroscope and Hardware Set Tray (sterilization tray)...

The Issue: The gravity steam, Ethylene Oxide (EO) and STERRAD 100S sterilization...

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

Class II — Potential Health HazardOngoing
DrugJune 18, 2012· Stat Rx USA

Recalled Item: Tobramycin Ophthalmic Oint. Recalled by Stat Rx USA Due to Labeling: Label...

The Issue: Labeling: Label Mix-up: The affected units were labeled incorrectly...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceJune 18, 2012· Safe N Simple, LLC

Recalled Item: Safe N Simple No-Sting Skin Barrier Film Recalled by Safe N Simple, LLC Due...

The Issue: The firm received a customer complaint of observed spots on the wipes. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2012· Synthes USA HQ, Inc.

Recalled Item: MIRS for MATRIX Spine System. Minimally Invasive Reduction Screw (MIRS)...

The Issue: Synthes is initiating a Medical Device Labeling Correction following a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Modular Perfusion System 9000 Recalled by Terumo Cardiovascular...

The Issue: Terumo Cardiovascular Systems has received several reports of malfunctions...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Modular Perfusion System 9000 Recalled by Terumo Cardiovascular...

The Issue: Terumo Cardiovascular Systems has received several reports of malfunctions...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Modular Perfusion System 8000 base Recalled by Terumo Cardiovascular...

The Issue: Terumo Cardiovascular Systems has received several reports of malfunctions...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2012· Varian Medical Systems, Inc. Oncology Systems

Recalled Item: Varian brand Varian Eclipse Treatment Planning System for radiotherapy...

The Issue: Varian has identified an anomaly with the Eclipse Treatment Planning (for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Modular Perfusion System 8000 base Recalled by Terumo Cardiovascular...

The Issue: Terumo Cardiovascular Systems has received several reports of malfunctions...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo Advanced Perfusion System 1. System 1 base 220/240V. The Recalled by...

The Issue: Terumo Cardiovascular Systems has received several reports of malfunctions...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Modular Perfusion System 8000 base Recalled by Terumo Cardiovascular...

The Issue: Terumo Cardiovascular Systems has received several reports of malfunctions...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Modular Perfusion System 8000 base Recalled by Terumo Cardiovascular...

The Issue: Terumo Cardiovascular Systems has received several reports of malfunctions...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Modular Perfusion System 9000 Recalled by Terumo Cardiovascular...

The Issue: Terumo Cardiovascular Systems has received several reports of malfunctions...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Modular Perfusion System 8000 base Recalled by Terumo Cardiovascular...

The Issue: Terumo Cardiovascular Systems has received several reports of malfunctions...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Modular Perfusion System 8000 base Recalled by Terumo Cardiovascular...

The Issue: Terumo Cardiovascular Systems has received several reports of malfunctions...

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

Class II — Potential Health HazardOngoing