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 4832148340 of 55,837 recalls

Medical DeviceFebruary 4, 2014· Focus Diagnostics Inc

Recalled Item: Simplexa Flu AlB & RSV Direct Assay Kits Recalled by Focus Diagnostics Inc...

The Issue: Focus Diagnostics initiated the recall of the certain Simplexa Flu AlB & RSV...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2014· Fresenius Medical Care Holdings, Inc.

Recalled Item: Optiflux F200NR High Flux Dialyzers Recalled by Fresenius Medical Care...

The Issue: Dialysate Port Leak During Priming of the Dialyzers

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2014· Fresenius Medical Care Holdings, Inc.

Recalled Item: Optiflux F18Nre Flux Dialyzers Recalled by Fresenius Medical Care Holdings,...

The Issue: Dialysate Port Leak During Priming of the Dialyzers

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2014· Fresenius Medical Care Holdings, Inc.

Recalled Item: Optiflux F200NRe High Flux Dialyzers Recalled by Fresenius Medical Care...

The Issue: Dialysate Port Leak During Priming of the Dialyzers

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2014· Fresenius Medical Care Holdings, Inc.

Recalled Item: Optiflux B200 Flux Dialyzers Recalled by Fresenius Medical Care Holdings,...

The Issue: Dialysate Port Leak During Priming of the Dialyzers

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2014· Fresenius Medical Care Holdings, Inc.

Recalled Item: Optiflux F160NRe High Flux Dialyzers Recalled by Fresenius Medical Care...

The Issue: Dialysate Port Leak During Priming of the Dialyzers

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2014· Philips Medical Systems, Inc.

Recalled Item: Philips HeartStart MRx Monitor/Defibrillator used Model numbers: M3535A...

The Issue: HeartStart MRx Defibrillator Monitor therapy connection could experience...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2014· Fresenius Medical Care Holdings, Inc.

Recalled Item: Optiflux F160NR High Flux Dialyzers Recalled by Fresenius Medical Care...

The Issue: Dialysate Port Leak During Priming of the Dialyzers

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2014· Fresenius Medical Care Holdings, Inc.

Recalled Item: Optiflux F180NR High Flux Dialyzers Recalled by Fresenius Medical Care...

The Issue: Dialysate Port Leak During Priming of the Dialyzers

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2014· Fresenius Medical Care Holdings, Inc.

Recalled Item: Optiflux F200A High Flux Dialyzers Recalled by Fresenius Medical Care...

The Issue: Dialysate Port Leak During Priming of the Dialyzers

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2014· Fresenius Medical Care Holdings, Inc.

Recalled Item: Optiflux F180NRe High Flux Dialyzers Recalled by Fresenius Medical Care...

The Issue: Dialysate Port Leak During Priming of the Dialyzers

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2014· Boston Scientific Corporation

Recalled Item: Boston Scientific Recalled by Boston Scientific Corporation Due to Boston...

The Issue: Boston Scientific is initiating this Recall Removal of one lot of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2014· Boston Scientific Corporation

Recalled Item: Boston Scientific Recalled by Boston Scientific Corporation Due to Boston...

The Issue: Boston Scientific is initiating this Recall Removal of one lot of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2014· Innovative Sterlization Technologies LLC

Recalled Item: OneTray Sealed Sterilization Containers Product Usage: A rigid sterilization...

The Issue: The wrong sterilization time was on the label. The label lists Steam Gravity...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2014· Hospira Inc.

Recalled Item: The GemStar Power Supply is an accessory for the GemStar Recalled by Hospira...

The Issue: The GemStar Infusion pump may not receive direct current (DC) power from the...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 3, 2014· Hospira Inc.

Recalled Item: The GemStar Power Supply is an accessory for the GemStar Recalled by Hospira...

The Issue: The GemStar Infusion pump may not receive direct current (DC) power from the...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 3, 2014· Altasource LLC dba Meta Labs LLC

Recalled Item: Hot Ice Recalled by Altasource LLC dba Meta Labs LLC Due to Firm is not...

The Issue: Firm is not registered as a drug manufacturer.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2014· Altasource LLC dba Meta Labs LLC

Recalled Item: Nice-En-Smooth Berry Burst Recalled by Altasource LLC dba Meta Labs LLC Due...

The Issue: Firm is not registered as a drug manufacturer.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2014· Altasource LLC dba Meta Labs LLC

Recalled Item: Amo-O Herbal Stimulator Recalled by Altasource LLC dba Meta Labs LLC Due to...

The Issue: Firm is not registered as a drug manufacturer.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2014· Altasource LLC dba Meta Labs LLC

Recalled Item: Mega-Gen His Personal Lubricant Recalled by Altasource LLC dba Meta Labs LLC...

The Issue: Firm is not registered as a drug manufacturer.

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

Class II — Potential Health HazardOngoing