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 4548145500 of 53,342 recalls

Medical DeviceMarch 5, 2014· ZOLL Medical Corporation

Recalled Item: Zoll Medical X Series Recalled by ZOLL Medical Corporation Due to...

The Issue: Defibrillator/Pacemaker/Monitor May Latch in a Continuous Device Reset Loop...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2014· Mevion Medical Systems, Inc.

Recalled Item: MEVION S250 Recalled by Mevion Medical Systems, Inc. Due to Geometric...

The Issue: Geometric positioning error can occur after a rotational correction has been...

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

Class II — Potential Health HazardOngoing
DrugMarch 4, 2014· Sagent Pharmaceuticals Inc

Recalled Item: Zoledronic Acid Injection 5 mg per 100 mL (0.05 mg/mL) Recalled by Sagent...

The Issue: Lack of Assurance of Sterility; leaking of premix bags

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 4, 2014· Alkermes, Inc.

Recalled Item: VIVITROL (naltrexone for extended-release injectable suspension) Recalled by...

The Issue: Customer complaints for failure to deliver the dose.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 4, 2014· Teva Pharmaceuticals USA

Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Teva Pharmaceuticals USA Due...

The Issue: Failed Tablet/Capsule Specifications: Teva Pharmaceuticals USA, is...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 4, 2014· Teva Pharmaceuticals USA

Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Teva Pharmaceuticals USA Due...

The Issue: Failed Tablet/Capsule Specifications: Teva Pharmaceuticals USA, is...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 4, 2014· Teva Pharmaceuticals USA

Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Teva Pharmaceuticals USA Due...

The Issue: Failed Tablet/Capsule Specifications: Teva Pharmaceuticals USA, is...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 4, 2014· House Of Flavors, Inc.

Recalled Item: Belmont Premium Ice Cream Recalled by House Of Flavors, Inc. Due to...

The Issue: may contain undeclared nut allergen.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMarch 4, 2014· Teleflex Medical

Recalled Item: Sengstaken Tube and Sengstaken-Blakemore Tube. Teleflex product codes 204800...

The Issue: Sterility of the product cannot be guaranteed.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2014· Thoratec Corporation

Recalled Item: HeartMate II System Controller Product Usage: HeartMate II is a Recalled by...

The Issue: Discovery of serious injuries and deaths associated with the process of...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 4, 2014· Thoratec Corporation

Recalled Item: HeartMate II LVAD Pump and Pock Controller Kit Recalled by Thoratec...

The Issue: Discovery of serious injuries and deaths associated with the process of...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 4, 2014· Thoratec Corporation

Recalled Item: Heart Mate II Pocket Controllers removed from packaging Product Usage:...

The Issue: Discovery of serious injuries and deaths associated with the process of...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 4, 2014· Thoratec Corporation

Recalled Item: HeartMate II Implant Kit with Pocket Controller Recalled by Thoratec...

The Issue: Discovery of serious injuries and deaths associated with the process of...

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

Class I — Serious Health HazardOngoing
DrugMarch 3, 2014· Terra-Medica Inc.

Recalled Item: Pleo Quent CAPSULES 4X Recalled by Terra-Medica Inc. Due to Penicillin Cross...

The Issue: Penicillin Cross Contamination

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 3, 2014· Terra-Medica Inc.

Recalled Item: Pleo Not PORTABLE SIPS Recalled by Terra-Medica Inc. Due to Penicillin Cross...

The Issue: Penicillin Cross Contamination

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 3, 2014· Terra-Medica Inc.

Recalled Item: Pleo Quent DROPS 5X Recalled by Terra-Medica Inc. Due to Penicillin Cross...

The Issue: Penicillin Cross Contamination

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 3, 2014· Terra-Medica Inc.

Recalled Item: Pleo Not PORTABLE SIPS Recalled by Terra-Medica Inc. Due to Penicillin Cross...

The Issue: Penicillin Cross Contamination

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 3, 2014· Terra-Medica Inc.

Recalled Item: Pleo Ex DROPS 5X Recalled by Terra-Medica Inc. Due to Penicillin Cross...

The Issue: Penicillin Cross Contamination

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 3, 2014· Terra-Medica Inc.

Recalled Item: Pleo Stolo DROPS 6X Recalled by Terra-Medica Inc. Due to Penicillin Cross...

The Issue: Penicillin Cross Contamination

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 3, 2014· Terra-Medica Inc.

Recalled Item: Pleo Not DROPS Recalled by Terra-Medica Inc. Due to Penicillin Cross...

The Issue: Penicillin Cross Contamination

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

Class II — Potential Health HazardOngoing
Refund