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. 2,424 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,424 in last 12 months

Showing 5024150260 of 53,342 recalls

DrugFebruary 13, 2013· Actavis Elizabeth LLC

Recalled Item: Dextroamphetamine Saccharate Recalled by Actavis Elizabeth LLC Due to Failed...

The Issue: Failed Dissolution Specification: This product recall is due to the product...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
FoodFebruary 13, 2013· Saratoga Therapeutics, LLC

Recalled Item: ebA*(TM) Multivitamin Supplement Recalled by Saratoga Therapeutics, LLC Due...

The Issue: The recall was initiated due to discovery of the presence of milk components...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 13, 2013· Rich Products Corp

Recalled Item: ALL NATURAL ANCIENT GRAIN BREAD Recalled by Rich Products Corp Due to...

The Issue: Product was manufactured with bulk flour supplied by Dakota Specialty...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 12, 2013· OLAAX International

Recalled Item: MAXILOSS Weight Advanced Recalled by OLAAX International Due to Marketed...

The Issue: Marketed Without an Approved NDA/ANDA: product contains sibutramine, a...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 12, 2013· Hospira Inc.

Recalled Item: 0.9% Sodium Chloride Irrigation Recalled by Hospira Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility: There is a potential for the solution to...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 12, 2013· Philips Medical Systems (Cleveland) Inc

Recalled Item: Intellispace Portal (ISP) Philips Medical Systems (Cleveland) Recalled by...

The Issue: Philips was notified of a problem using the IntelliSpace Portal with...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2013· Beckman Coulter Inc.

Recalled Item: Access Immunoassay System Recalled by Beckman Coulter Inc. Due to Beckman...

The Issue: Beckman Coulter is initiating a recall due to a defective newly released...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2013· Polymedco, Inc

Recalled Item: Test Strips packaged in the OC-Light Manual iFOBT Kit Recalled by Polymedco,...

The Issue: The test strips in the affected product lots of the OC Light immunological...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2013· Beckman Coulter Inc.

Recalled Item: Access 2 Immunoassay System Recalled by Beckman Coulter Inc. Due to Beckman...

The Issue: Beckman Coulter is initiating a recall due to a defective newly released...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2013· Polymedco, Inc

Recalled Item: Test Strips packaged in the OC-Light Manual iFOBT Kit Recalled by Polymedco,...

The Issue: The test strips in the affected product lots of the OC Light immunological...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2013· Beckman Coulter Inc.

Recalled Item: UniCel DxC 600i Synchron Access Clinical System Recalled by Beckman Coulter...

The Issue: Beckman Coulter is initiating a recall due to a defective newly released...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2013· Beckman Coulter Inc.

Recalled Item: Synchron LXi 725 Clinical System Recalled by Beckman Coulter Inc. Due to...

The Issue: Beckman Coulter is initiating a recall due to a defective newly released...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2013· Steris Corporation

Recalled Item: AMSCO C and AMSCO 400 Steam Sterilizers designed for sterilization Recalled...

The Issue: The control boards alarm set points and temperature tolerances allowed for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2013· Integra LifeSciences Corp.

Recalled Item: Integra(R) Jarit(R) Monopolar Cable (Catalogue No. 600-290). For use in...

The Issue: Addendum to the Instructions for Use. The addendum emphasizes the warnings...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2013· Oculus Innovative Sciences Inc

Recalled Item: Atrapro Antipruritic Hydrogel Recalled by Oculus Innovative Sciences Inc Due...

The Issue: Out of specification result - stability test failure of free available...

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

Class II — Potential Health HazardOngoing
DrugFebruary 11, 2013· Jubilant Cadista Pharmaceuticals Inc.

Recalled Item: Pantoprazole Sodium Delayed Release Tablets USP Recalled by Jubilant Cadista...

The Issue: cGMP Deviations: Oral products were not manufactured in accordance with Good...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 11, 2013· Innominata Dba Genbio

Recalled Item: ANTI-BORRELIA (LYME) MICROPLATE EIA Kit Recalled by Innominata Dba Genbio...

The Issue: Multiple incidents of low-reacting assay plates.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2013· Elekta, Inc.

Recalled Item: Monaco RTP System. Radiation treatment planning. Recalled by Elekta, Inc....

The Issue: The beam is displayed at the "gantry" angle, but the dose is calculated at...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2013· Zimmer Biomet, Inc.

Recalled Item: ROSA Surgical Device 2.5.8 Recalled by Zimmer Biomet, Inc. Due to Issue with...

The Issue: Issue with optional neuro-endoscopy module detected under specific...

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

Class II — Potential Health HazardOngoing
DrugFebruary 8, 2013· Watson Laboratories Inc

Recalled Item: Meprobamate Recalled by Watson Laboratories Inc Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Watson Laboratories Inc. is...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund