Product Recalls in Alabama

Product recalls affecting Alabama — including food, drugs, consumer products, medical devices, and vehicles distributed to Alabama. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,467 recalls have been distributed to Alabama in the last 12 months.

50,591 total recalls
2,467 in last 12 months

Showing 2494124960 of 28,641 recalls

Medical DeviceFebruary 5, 2014· Synthes, Inc.

Recalled Item: Synthes 5.0mm Variable Locking Screw This device is part of Recalled by...

The Issue: Labeling correction: The package insert in one 5.0mm Variable Locking Screw...

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· 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 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 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 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· 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· 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· 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· 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· 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 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· 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 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 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· 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· Stryker Howmedica Osteonics Corp.

Recalled Item: Citation TMZF HA 132 degrees Neck Angle Recalled by Stryker Howmedica...

The Issue: Stryker received a report from the field indicating that a citation TMZF HA...

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
Medical DeviceFebruary 3, 2014· Siemens Medical Solutions Diagnostics

Recalled Item: IMMULITE 2000 Recalled by Siemens Medical Solutions Diagnostics Due to There...

The Issue: There is a potential for incorrect results to be reported from processing of...

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