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. 2,492 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,492 in last 12 months

Showing 3926139280 of 53,342 recalls

Medical DeviceJuly 27, 2015· Transonic Systems Inc

Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...

The Issue: Software defect; programming errors in the blood flow probes EPROM....

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Transonic Systems Inc

Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...

The Issue: Software defect; programming errors in the blood flow probes EPROM....

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Transonic Systems Inc

Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...

The Issue: Software defect; programming errors in the blood flow probes EPROM....

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Transonic Systems Inc

Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...

The Issue: Software defect; programming errors in the blood flow probes EPROM....

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur¿ Folate Ascorbic Acid/Ascorbic Acid Diluent Recalled by...

The Issue: Low red blood cell control recoveries and low results for red blood cell...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Transonic Systems Inc

Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...

The Issue: Software defect; programming errors in the blood flow probes EPROM....

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Transonic Systems Inc

Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...

The Issue: Software defect; programming errors in the blood flow probes EPROM....

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Transonic Systems Inc

Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...

The Issue: Software defect; programming errors in the blood flow probes EPROM....

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Transonic Systems Inc

Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...

The Issue: Software defect; programming errors in the blood flow probes EPROM....

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Transonic Systems Inc

Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...

The Issue: Software defect; programming errors in the blood flow probes EPROM....

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

Class II — Potential Health HazardOngoing
FoodJuly 27, 2015· Christie Cookie Co Inc

Recalled Item: Doubletree Cookie Dough Recalled by Christie Cookie Co Inc Due to Reports of...

The Issue: Reports of clear and green plastic pieces in cookies.

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 25, 2015· The Kroger Co

Recalled Item: Kroger Ground Cinnamon NEW WT. 18.3 oz Plastic container Recalled by The...

The Issue: The products were recalled because a container of Kroger Garlic Powder...

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 25, 2015· The Kroger Co

Recalled Item: Kroger Black Pepper Coarse Ground NET WT Recalled by The Kroger Co Due to...

The Issue: The products were recalled because a container of Kroger Garlic Powder...

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 25, 2015· The Kroger Co

Recalled Item: Kroger Bac'n Buds ARTIFICIAL BACON FLAVORED CHIPS 14.1oz plastic container...

The Issue: The products were recalled because a container of Kroger Garlic Powder...

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 25, 2015· The Kroger Co

Recalled Item: Kroger Garlic Powder NEW WT 24.7 OZ Plastic Container Recalled by The Kroger...

The Issue: The products were recalled because a container of Kroger Garlic Powder...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 24, 2015· Medtronic Perfusion Systems

Recalled Item: Medtronic EOPA Arterial Cannula Recalled by Medtronic Perfusion Systems Due...

The Issue: EOPA Arterial Cannula Devices in this lot were shipped without the guidewire.

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

Class II — Potential Health HazardOngoing
DrugJuly 24, 2015· Boehringer Ingelheim Roxane Inc

Recalled Item: COMBIVENT RESPIMAT (ipratropium bromide and albuterol) Inhalation Spray...

The Issue: Defective Delivery System: Inhalers do not spray properly, emitting either...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 24, 2015· Shionogi Inc.

Recalled Item: Nisoldipine Extended Release Tablets Recalled by Shionogi Inc. Due to Failed...

The Issue: Failed Dissolution Specifications

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

Class III — Low RiskOngoing
Refund
DrugJuly 24, 2015· Ucb, Inc

Recalled Item: univasc (moexipril HCl) tablets Recalled by Ucb, Inc Due to Failed...

The Issue: Failed Dissolution Testing: Failed 24 month dissolution testing.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 24, 2015· Teva Pharmaceuticals USA

Recalled Item: ADRUCIL (fluorouracil injection Recalled by Teva Pharmaceuticals USA Due to...

The Issue: Presence of Particulate Matter: silcone rubber and fluorouracil crystals...

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

Class I — Serious Health HazardOngoing
Refund