Product Recalls in Michigan

Product recalls affecting Michigan — including food, drugs, consumer products, medical devices, and vehicles distributed to Michigan. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,520 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,520 in last 12 months

Showing 2560125620 of 29,286 recalls

Medical DeviceFebruary 7, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Zee Angiographic x-ray systems. Recalled by Siemens Medical Solutions...

The Issue: An inappropriate cable connection was assembled for certain Artis zee...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2014· GE Healthcare, LLC

Recalled Item: Elscint APEX Helix Recalled by GE Healthcare, LLC Due to Potential safety...

The Issue: Potential safety issue related to unintended radial detector motion, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2014· Medtronic Vascular

Recalled Item: Medtronic Everest 20cc Inflation Device Recalled by Medtronic Vascular Due...

The Issue: Incorrect master label.

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

Class III — Low RiskOngoing
Medical DeviceFebruary 6, 2014· Philips Medical Systems North America Inc.

Recalled Item: Philips HeartStart FR3 Automated External Defibrillator (AED) Recalled by...

The Issue: Philip's is recalling HeartStart FR3 Automated External Defibrillator (AED)...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2014· Philips Medical Systems North America Inc.

Recalled Item: Philips HeartStart Home and OnSite (HS1) automated external defibrillators...

The Issue: Philips is recalling HeartStart Home and OnSite (HS1) automated external...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2014· Fisher Scientific Co

Recalled Item: Fisherbrand Sterile Swabs Recalled by Fisher Scientific Co Due to A customer...

The Issue: A customer reported the presence of an organism in a lot of Calcium Alginate...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2014· Alere San Diego, Inc.

Recalled Item: Product Brand Name(s): Alere Triage¿ TOX+MTD Drug Screen Recalled by Alere...

The Issue: Alere San Diego, Inc. is initiating a recall of the Alere Triage¿ TOX Drug...

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

Class II — Potential Health HazardOngoing
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· 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 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· 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 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· 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