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. 2,815 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
2,815 in last 12 months

Showing 1702117040 of 30,686 recalls

Medical DeviceMay 4, 2018· Thermo Fisher

Recalled Item: remel SUPERPACK CS/ 500 SEG/FLASK Recalled by Thermo Fisher Due to Product...

The Issue: Product may fail performance testing for S aureus ATCC 43300.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2018· Synthes (USA) Products LLC

Recalled Item: Synthes Torque Limiting Handle Recalled by Synthes (USA) Products LLC Due to...

The Issue: The adapter may demonstrate a degradation of function as the final products...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2018· Medtronic Neurosurgery

Recalled Item: Medtronic Clip Gun Magazines are packaged in individually sealed pouches...

The Issue: The packaging sterile barrier does not comply with the applicable packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2018· Ethicon Endo-Surgery Inc

Recalled Item: HARMONIC ACE Shears + Adaptive Tissue Technology Recalled by Ethicon...

The Issue: The devices may have been assembled with an internal component that may...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2018· Maquet Datascope Corp - Cardiac Assist Division

Recalled Item: CARDIOSAVE Hybrid Intra-Aortic Balloon Pump (IABP) Recalled by Maquet...

The Issue: Ingress of fluids into the device can affect various electronic circuit...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 3, 2018· Joerns Healthcare

Recalled Item: P.R.O. Matt: (a) PROMATT PLUS 36 X 76 MATRESS Recalled by Joerns Healthcare...

The Issue: Joerns Healthcare has identified a potential issue with some of the P.R.O....

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2018· Joerns Healthcare

Recalled Item: ProCair Mattress: (a) PROCAIR PLUS 42X80 Recalled by Joerns Healthcare Due...

The Issue: Joerns Healthcare has identified a potential issue with some of the P.R.O....

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2018· Ethicon Endo-Surgery Inc

Recalled Item: HARMONIC ACE Shears + Adaptive Tissue Technology Recalled by Ethicon...

The Issue: The devices may have been assembled with an internal component that may...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2018· Galt Medical Corporation

Recalled Item: 1) Drainer Centesis Catheter Recalled by Galt Medical Corporation Due to The...

The Issue: The products listed might contain unsafe levels of bacterial endotoxins...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2018· Galt Medical Corporation

Recalled Item: Centeze Centesis Catheter Recalled by Galt Medical Corporation Due to The...

The Issue: The products listed might contain unsafe levels of bacterial endotoxins...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2018· Galt Medical Corporation

Recalled Item: Tearaway Introducers Recalled by Galt Medical Corporation Due to The...

The Issue: The products listed might contain unsafe levels of bacterial endotoxins...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2018· Galt Medical Corporation

Recalled Item: Elite HV Introducer Recalled by Galt Medical Corporation Due to The products...

The Issue: The products listed might contain unsafe levels of bacterial endotoxins...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2018· Galt Medical Corporation

Recalled Item: 1) TVS LPA Recalled by Galt Medical Corporation Due to The products listed...

The Issue: The products listed might contain unsafe levels of bacterial endotoxins...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2018· Galt Medical Corporation

Recalled Item: 1) ELITE HV Recalled by Galt Medical Corporation Due to The products listed...

The Issue: The products listed might contain unsafe levels of bacterial endotoxins...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2018· Galt Medical Corporation

Recalled Item: TVS LPA Recalled by Galt Medical Corporation Due to The products listed...

The Issue: The products listed might contain unsafe levels of bacterial endotoxins...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2018· Galt Medical Corporation

Recalled Item: 1) Vascular Dilator Recalled by Galt Medical Corporation Due to The products...

The Issue: The products listed might contain unsafe levels of bacterial endotoxins...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2018· Ad-Tech Medical Instrument Corporation

Recalled Item: AD-TECH Medical Instrument Corporation Drill Sleeve Guides DSG-6-3-090-2.4N...

The Issue: The diameter of the drill sleeve guide raw material was found to be under...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2018· The Seaberg Company Inc

Recalled Item: Part #: SAM XT-M Recalled by The Seaberg Company Inc Due to Based on...

The Issue: Based on internal testing, results indicated a possible failure of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2018· The Seaberg Company Inc

Recalled Item: Part #: SAM XT-C Recalled by The Seaberg Company Inc Due to Based on...

The Issue: Based on internal testing, results indicated a possible failure of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2018· The Seaberg Company Inc

Recalled Item: Part #: SAM XT-C Recalled by The Seaberg Company Inc Due to Based on...

The Issue: Based on internal testing, results indicated a possible failure of the...

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

Class II — Potential Health HazardOngoing