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 3292132940 of 53,342 recalls

Medical DeviceJanuary 3, 2017· Stryker Leibinger GmbH & Co. KG

Recalled Item: 9805 Orbital Volume Sizer Set with Tray (Non-sterile) 9951 Design Recalled...

The Issue: An incorrect sterility status on the label, non-sterile products labeled as...

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

Class II — Potential Health HazardOngoing
FoodJanuary 3, 2017· High Liner Foods, Inc.

Recalled Item: FPI Breaded Round Shrimp Tail-On 1001990 Recalled by High Liner Foods, Inc....

The Issue: Product contains undeclared milk and eggs

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 1, 2017· BioMerieux SA

Recalled Item: Ceftriaxone TX 32 US S30 Recalled by BioMerieux SA Due to Potential...

The Issue: Potential performance issue on strain categorization.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 30, 2016· Hospira Inc., A Pfizer Company

Recalled Item: Plum 360 Infusion Pump Recalled by Hospira Inc., A Pfizer Company Due to...

The Issue: Depleted Battery alarm shows instead of Replace Battery. On battery power,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 29, 2016· Synthes (USA) Products LLC

Recalled Item: Synthes Radial Head Prosthesis System Recalled by Synthes (USA) Products LLC...

The Issue: There is the possibility that the radial stem may loosen post-operatively at...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 28, 2016· Medtronic Advanced Energy, LLC

Recalled Item: Intact Disposable Wands (part of the Intact System) 777-115BT: 5 Recalled by...

The Issue: Product sterility compromised due to breach of sterile barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 28, 2016· Medtronic Advanced Energy, LLC

Recalled Item: Intact Disposable Wands (part of the Intact System) 777-120: 5 Recalled by...

The Issue: Product sterility compromised due to breach of sterile barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 28, 2016· Medtronic Advanced Energy, LLC

Recalled Item: Intact Disposable Wands (part of the Intact System) 777-112: 5 Recalled by...

The Issue: Product sterility compromised due to breach of sterile barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 28, 2016· Medtronic Advanced Energy, LLC

Recalled Item: Intact Disposable Wands (part of the Intact System) 777-120BT: 5 Recalled by...

The Issue: Product sterility compromised due to breach of sterile barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 28, 2016· Medtronic Advanced Energy, LLC

Recalled Item: Intact Disposable Wands (part of the Intact System) 900-115: 5 Recalled by...

The Issue: Product sterility compromised due to breach of sterile barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 28, 2016· Medtronic Advanced Energy, LLC

Recalled Item: Intact Disposable Wands (part of the Intact System) 777-110: 5 Recalled by...

The Issue: Product sterility compromised due to breach of sterile barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 28, 2016· Medtronic Advanced Energy, LLC

Recalled Item: Intact Disposable Wands (part of the Intact System) 900-112: 5 Recalled by...

The Issue: Product sterility compromised due to breach of sterile barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 28, 2016· Medtronic Advanced Energy, LLC

Recalled Item: Intact Disposable Wands (part of the Intact System) 900-120: 5 Recalled by...

The Issue: Product sterility compromised due to breach of sterile barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 28, 2016· Medtronic Advanced Energy, LLC

Recalled Item: Intact Disposable Wands (part of the Intact System) 777-112BT: 5 Recalled by...

The Issue: Product sterility compromised due to breach of sterile barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 28, 2016· Medtronic Advanced Energy, LLC

Recalled Item: Intact Disposable Wands (part of the Intact System) 900-130: 5 Recalled by...

The Issue: Product sterility compromised due to breach of sterile barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 28, 2016· Medtronic Advanced Energy, LLC

Recalled Item: Intact Disposable Wands (part of the Intact System) 777-115: 5 Recalled by...

The Issue: Product sterility compromised due to breach of sterile barrier

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

Class II — Potential Health HazardOngoing
DrugDecember 28, 2016· Dr. Reddy's Laboratories, Inc.

Recalled Item: Flucanozole Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...

The Issue: Failed Dissolution Specifications; 18 month stability time point

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 28, 2016· Dr. Reddy's Laboratories, Inc.

Recalled Item: Flucanozole Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...

The Issue: Failed Dissolution Specifications; 18 month stability time point

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 28, 2016· L. Perrigo Company

Recalled Item: Clindamycin Phosphate and Benzoyl Peroxide Gel Recalled by L. Perrigo...

The Issue: Microbial Contamination of Non-Sterile Product; small number of tubes may...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 28, 2016· Dr. Reddy's Laboratories, Inc.

Recalled Item: Flucanozole Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...

The Issue: Failed Dissolution Specifications; 18 month stability time point

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

Class II — Potential Health HazardOngoing
Refund