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. 939 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
939 in last 12 months

Showing 46121–46140 of 53,342 recalls

FoodNovember 22, 2013· Senor Murphy Candymaker, LLC

Recalled Item: Senor Murphy Santa Fe Candymaker Peanut Brittle Recalled by Senor Murphy...

The Issue: Senor Murphy Candymaker is recalling Pecan Bueno, Cashew Crunch, Chile...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 22, 2013· Senor Murphy Candymaker, LLC

Recalled Item: Senor Murphy Santa Fe Candymaker Chile Pistachio Bark Recalled by Senor...

The Issue: Senor Murphy Candymaker is recalling Pecan Bueno, Cashew Crunch, Chile...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 22, 2013· Threshold Enterprises Ltd

Recalled Item: Source Naturals Essential Enzyme Ultra VEGI-CAP: Premium Digestive Enzyme...

The Issue: Dietary Supplements were made with bulk products provided by National Enzyme...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 22, 2013· Senor Murphy Candymaker, LLC

Recalled Item: Senor Murphy Santa Fe Candymaker Chili Peanut Brittle Recalled by Senor...

The Issue: Senor Murphy Candymaker is recalling Pecan Bueno, Cashew Crunch, Chile...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 22, 2013· Senor Murphy Candymaker, LLC

Recalled Item: Senor Murphy Santa Fe Candymaker Pinon Brittle Recalled by Senor Murphy...

The Issue: Senor Murphy Candymaker is recalling Pecan Bueno, Cashew Crunch, Chile...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 22, 2013· Senor Murphy Candymaker, LLC

Recalled Item: Senor Murphy Santa Fe Candymaker Cashew Crunch Recalled by Senor Murphy...

The Issue: Senor Murphy Candymaker is recalling Pecan Bueno, Cashew Crunch, Chile...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 22, 2013· Senor Murphy Candymaker, LLC

Recalled Item: Senor Murphy Santa Fe Candymaker Pecan Bueno Recalled by Senor Murphy...

The Issue: Senor Murphy Candymaker is recalling Pecan Bueno, Cashew Crunch, Chile...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 22, 2013· Senor Murphy Candymaker, LLC

Recalled Item: Senor Murphy Santa Fe Candymaker Chile Peanuts Recalled by Senor Murphy...

The Issue: Senor Murphy Candymaker is recalling Pecan Bueno, Cashew Crunch, Chile...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 21, 2013· Neuro Kinetics, Inc.

Recalled Item: Normative Data Template CD for use with the I-Portal devices. Used to...

The Issue: The data provided on the Normative Data Template CD for use with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2013· Medrad Mr Inc

Recalled Item: Medrad Veris MR Monitor units The system is intended to Recalled by Medrad...

The Issue: The main board, P/N 301641, installed in some Medrad Veris MR Monitor units...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2013· Ziehm Imaging Inc

Recalled Item: Ziehm Vista/Vista Plus C-Arm Interventional Fluoroscopic X-Ray System....

The Issue: Engineering change in 2006 resulted in a minor non-conformity of their...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2013· Ziehm Imaging Inc

Recalled Item: Ziehm Vision C-Arm Interventional Fluoroscopic X-Ray System. Mobile...

The Issue: Engineering change in 2006 resulted in a minor non-conformity of their...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2013· Ziehm Imaging Inc

Recalled Item: Ziehm Vision(2) FD C-Arm Interventional Fluoroscopic X-Ray System. Mobile...

The Issue: Engineering change in 2006 resulted in a minor non-conformity of their...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2013· Welch Allyn Protocol, Inc

Recalled Item: The Propaq LT Series monitors. Model numbers 802LTAN Recalled by Welch Allyn...

The Issue: Welch Allyn will update Propaq 802 Series Vital Signs Monitor, models are...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2013· Steris Corporation

Recalled Item: SYSTEM 1E Liquid Chemical Sterilant Processing System Recalled by Steris...

The Issue: Customers indicated fluctuations in environmental conditions sites and...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2013· Ziehm Imaging Inc

Recalled Item: Ziehm Vision(2) C-Arm Interventional Fluoroscopic X-Ray System. Mobile...

The Issue: Engineering change in 2006 resulted in a minor non-conformity of their...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2013· 3M Company - Health Care Business

Recalled Item: 3M ESPE Imprint II Regular Body Recalled by 3M Company - Health Care...

The Issue: Specific lots of Imprint II and Paradigm impression material packs are being...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2013· Remel Inc

Recalled Item: Oxoid Antimicrobial Susceptibility Testing Disc Recalled by Remel Inc Due to...

The Issue: Individual discs in the lot may not be sufficiently impregnated with...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2013· Ziehm Imaging Inc

Recalled Item: Ziehm Vision RFD C-Arm Interventional Fluoroscopic X-Ray System. Mobile...

The Issue: Engineering change in 2006 resulted in a minor non-conformity of their...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2013· Ziehm Imaging Inc

Recalled Item: Ziehm Vision R C-Arm Interventional Fluoroscopic X-Ray System. Mobile...

The Issue: Engineering change in 2006 resulted in a minor non-conformity of their...

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

Class II — Potential Health HazardOngoing