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. 2,832 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
2,832 in last 12 months

Showing 1544115460 of 30,686 recalls

Medical DeviceDecember 21, 2018· Philips Medical Systems Nederlands

Recalled Item: Achieva 3.0T Recalled by Philips Medical Systems Nederlands Due to There is...

The Issue: There is a potential for the ceiling speaker(s) to fall from their position...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2018· Philips Medical Systems Nederlands

Recalled Item: Ingenia Ambition S Recalled by Philips Medical Systems Nederlands Due to...

The Issue: There is a potential for the ceiling speaker(s) to fall from their position...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2018· Philips Medical Systems Nederlands

Recalled Item: MR-OR 1.5T Recalled by Philips Medical Systems Nederlands Due to There is a...

The Issue: There is a potential for the ceiling speaker(s) to fall from their position...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2018· Philips Medical Systems Nederlands

Recalled Item: Achieva 3.0T for PET Recalled by Philips Medical Systems Nederlands Due to...

The Issue: There is a potential for the ceiling speaker(s) to fall from their position...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2018· Philips Medical Systems Nederlands

Recalled Item: Panorama 1.0T Recalled by Philips Medical Systems Nederlands Due to There is...

The Issue: There is a potential for the ceiling speaker(s) to fall from their position...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2018· Philips Medical Systems Nederlands

Recalled Item: Intera 0.5T Standard Recalled by Philips Medical Systems Nederlands Due to...

The Issue: There is a potential for the ceiling speaker(s) to fall from their position...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2018· Philips Medical Systems Nederlands

Recalled Item: Achieva 1.5T Recalled by Philips Medical Systems Nederlands Due to There is...

The Issue: There is a potential for the ceiling speaker(s) to fall from their position...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2018· Philips Medical Systems Nederlands

Recalled Item: Intera 1.5T High Performance Recalled by Philips Medical Systems Nederlands...

The Issue: There is a potential for the ceiling speaker(s) to fall from their position...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2018· Draeger Medical, Inc.

Recalled Item: ID Circuit Basic 180 Recalled by Draeger Medical, Inc. Due to Incorrectly...

The Issue: Incorrectly pre-assembled breathing circuit has potential for incorrect...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 21, 2018· Draeger Medical, Inc.

Recalled Item: VentStar Watertrap (P) 180 Recalled by Draeger Medical, Inc. Due to...

The Issue: Incorrectly pre-assembled breathing circuit has potential for incorrect...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 21, 2018· Draeger Medical, Inc.

Recalled Item: VentStar Basic 250 Recalled by Draeger Medical, Inc. Due to Incorrectly...

The Issue: Incorrectly pre-assembled breathing circuit has potential for incorrect...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 21, 2018· Draeger Medical, Inc.

Recalled Item: ID Circuit Watertrap (P) 180 Recalled by Draeger Medical, Inc. Due to...

The Issue: Incorrectly pre-assembled breathing circuit has potential for incorrect...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 21, 2018· Draeger Medical, Inc.

Recalled Item: VentStar Basic (P) 250 Recalled by Draeger Medical, Inc. Due to Incorrectly...

The Issue: Incorrectly pre-assembled breathing circuit has potential for incorrect...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 21, 2018· Draeger Medical, Inc.

Recalled Item: VentStar Basic 180 Recalled by Draeger Medical, Inc. Due to Incorrectly...

The Issue: Incorrectly pre-assembled breathing circuit has potential for incorrect...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 21, 2018· Draeger Medical, Inc.

Recalled Item: VentStar Basic (P) 180 Recalled by Draeger Medical, Inc. Due to Incorrectly...

The Issue: Incorrectly pre-assembled breathing circuit has potential for incorrect...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 21, 2018· Draeger Medical, Inc.

Recalled Item: ID Circuit Basic 250 Recalled by Draeger Medical, Inc. Due to Incorrectly...

The Issue: Incorrectly pre-assembled breathing circuit has potential for incorrect...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 21, 2018· Draeger Medical, Inc.

Recalled Item: VentStar Anesthesia WT(P) 180 Recalled by Draeger Medical, Inc. Due to...

The Issue: Incorrectly pre-assembled breathing circuit has potential for incorrect...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 20, 2018· Steris Corporation

Recalled Item: AMSCO 5000 Series Washer/Disinfector Model # 5052 Recalled by Steris...

The Issue: The software in the systems may not process the cycle originally intended....

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2018· Steris Corporation

Recalled Item: AMSCO 3000 Series Washer/Disinfector Model # 3052 Recalled by Steris...

The Issue: The software in the systems may not process the cycle originally intended....

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2018· Becton Dickinson & Co.

Recalled Item: Phoenix AST Indicator Recalled by Becton Dickinson & Co. Due to Panels...

The Issue: Panels inoculated using certain lots of the indicator solution are...

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

Class II — Potential Health HazardOngoing