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. 2,441 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,441 in last 12 months

Showing 4556145580 of 53,342 recalls

Medical DeviceFebruary 24, 2014· Nico Corp.

Recalled Item: Myriad handpiece Tissue morcellator Recalled by Nico Corp. Due to This...

The Issue: This recall has been initiated due to a defective component within the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2014· Allesee Orthodontic Appliances

Recalled Item: AOA Distalizer Lock Nut Screw Recalled by Allesee Orthodontic Appliances Due...

The Issue: The Lock Nut component of the Jet appliances may be missing the screw...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2014· DePuy Orthopaedics, Inc.

Recalled Item: R S-ROM Noiles Rotating Hinge Recalled by DePuy Orthopaedics, Inc. Due to...

The Issue: DePuy Orthopaedics has identified the potential for holes to develop in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2014· DePuy Orthopaedics, Inc.

Recalled Item: R Recalled by DePuy Orthopaedics, Inc. Due to DePuy Orthopaedics has...

The Issue: DePuy Orthopaedics has identified the potential for holes to develop in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2014· DePuy Orthopaedics, Inc.

Recalled Item: L Recalled by DePuy Orthopaedics, Inc. Due to DePuy Orthopaedics has...

The Issue: DePuy Orthopaedics has identified the potential for holes to develop in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2014· DePuy Orthopaedics, Inc.

Recalled Item: L S-ROM Noiles Rotating Hinge Recalled by DePuy Orthopaedics, Inc. Due to...

The Issue: DePuy Orthopaedics has identified the potential for holes to develop in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2014· DePuy Orthopaedics, Inc.

Recalled Item: L S-ROM Noiles Rotating Hinge Recalled by DePuy Orthopaedics, Inc. Due to...

The Issue: DePuy Orthopaedics has identified the potential for holes to develop in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2014· DePuy Orthopaedics, Inc.

Recalled Item: RS-ROM Noiles Rotating Hinge Recalled by DePuy Orthopaedics, Inc. Due to...

The Issue: DePuy Orthopaedics has identified the potential for holes to develop in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2014· Medical Information Technology, Inc.

Recalled Item: MEDITECH Microbiology Recalled by Medical Information Technology, Inc. Due...

The Issue: Potential for erroneous result reporting.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2014· DeRoyal Industries Inc

Recalled Item: DeRoyal(R) LIMB HOLDERS Recalled by DeRoyal Industries Inc Due to Moldy...

The Issue: Moldy smell in product

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

Class II — Potential Health HazardOngoing
DrugFebruary 20, 2014· GlaxoSmithKline Consumer Healthcare; dba-GlaxoSmithKline

Recalled Item: Nicorette Lozenge and NicoDerm CQ Recalled by GlaxoSmithKline Consumer...

The Issue: Failed Lozenge Specifications; Lozenges are overly thick, overly soft, and...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 20, 2014· GlaxoSmithKline Consumer Healthcare; dba-GlaxoSmithKline

Recalled Item: Nicotine polacrilex lozenge Recalled by GlaxoSmithKline Consumer Healthcare;...

The Issue: Failed Lozenge Specifications; Lozenges are overly thick, overly soft, and...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 20, 2014· GlaxoSmithKline Consumer Healthcare; dba-GlaxoSmithKline

Recalled Item: Nicorette Lozenge Recalled by GlaxoSmithKline Consumer Healthcare;...

The Issue: Failed Lozenge Specifications; Lozenges are overly thick, overly soft, and...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 20, 2014· GlaxoSmithKline Consumer Healthcare; dba-GlaxoSmithKline

Recalled Item: Nicorette (nicotine polacrilex) Lozenges Mini Recalled by GlaxoSmithKline...

The Issue: Failed Lozenge Specifications; Lozenges are overly thick, overly soft, and...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 20, 2014· GlaxoSmithKline Consumer Healthcare; dba-GlaxoSmithKline

Recalled Item: Nicotine polacrilex lozenge Recalled by GlaxoSmithKline Consumer Healthcare;...

The Issue: Failed Lozenge Specifications; Lozenges are overly thick, overly soft, and...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 20, 2014· GlaxoSmithKline Consumer Healthcare; dba-GlaxoSmithKline

Recalled Item: Nicotine polacrilex lozenge Recalled by GlaxoSmithKline Consumer Healthcare;...

The Issue: Failed Lozenge Specifications; Lozenges are overly thick, overly soft, and...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 20, 2014· GlaxoSmithKline Consumer Healthcare; dba-GlaxoSmithKline

Recalled Item: Nicorette (nicotine polacrilex) Lozenges Mini Recalled by GlaxoSmithKline...

The Issue: Failed Lozenge Specifications; Lozenges are overly thick, overly soft, and...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 20, 2014· GlaxoSmithKline Consumer Healthcare; dba-GlaxoSmithKline

Recalled Item: Nicotine polacrilex lozenge Recalled by GlaxoSmithKline Consumer Healthcare;...

The Issue: Failed Lozenge Specifications; Lozenges are overly thick, overly soft, and...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 20, 2014· GlaxoSmithKline Consumer Healthcare; dba-GlaxoSmithKline

Recalled Item: Nicotine polacrilex lozenge Recalled by GlaxoSmithKline Consumer Healthcare;...

The Issue: Failed Lozenge Specifications; Lozenges are overly thick, overly soft, and...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 20, 2014· GlaxoSmithKline Consumer Healthcare; dba-GlaxoSmithKline

Recalled Item: Nicotine polacrilex lozenge Recalled by GlaxoSmithKline Consumer Healthcare;...

The Issue: Failed Lozenge Specifications; Lozenges are overly thick, overly soft, and...

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

Class III — Low RiskOngoing
Refund