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. 2,498 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,498 in last 12 months

Showing 3700137020 of 53,342 recalls

DrugFebruary 4, 2016· Hartley Medical Center Pharmacy, Incorporated

Recalled Item: Hydromorphone HCL 10 mg/ml/Fentanyl Citrate 0.15 mg/ml Recalled by Hartley...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 4, 2016· Hartley Medical Center Pharmacy, Incorporated

Recalled Item: Hydromorphone HCL 2 mg/ml Recalled by Hartley Medical Center Pharmacy,...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 4, 2016· Hartley Medical Center Pharmacy, Incorporated

Recalled Item: Baclofen 5000 mcg/ml Recalled by Hartley Medical Center Pharmacy,...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 4, 2016· Hartley Medical Center Pharmacy, Incorporated

Recalled Item: Sufentanil Cit 200 mcg/ml/Clonidine HCL 1600 mcg/ml Recalled by Hartley...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 4, 2016· Hartley Medical Center Pharmacy, Incorporated

Recalled Item: Hydromorphone HCL 10 mg/ml/Bupivacaine HCL 4 mg/ml Recalled by Hartley...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 4, 2016· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens Healthcare Diagnostics ADVIA Centaur Calibrator E- 6- Pack Catalog...

The Issue: ADVIA Centaur Systems Calibrator E Lot 42 and 43 Bias with the Testosterone...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: (Stryker) AccuPlace Round Level Needle Guide Recalled by Stryker Instruments...

The Issue: During an evaluation of the product packaging, it was determined that there...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: (Stryker) AccuPlace Straight Level Needle Guide Recalled by Stryker...

The Issue: During an evaluation of the product packaging, it was determined that there...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 50000 (Inrad) AccuPlace Drace Stereotaxic Needle Guide Recalled by Stryker...

The Issue: During an evaluation of the product packaging, it was determined that there...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 50001 (Inrad) AccuPlace Drace Stereotaxic Needle Guide Recalled by Stryker...

The Issue: During an evaluation of the product packaging, it was determined that there...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2016· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens Healthcare Diagnostics ADVIA Centaur Calibrator E - 2-Pack Catalog...

The Issue: ADVIA Centaur Systems Calibrator E Lot 42 and 43 Bias with the Testosterone...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2016· Draeger Medical, Inc.

Recalled Item: Evita Infinity V500 Ventilator Recalled by Draeger Medical, Inc. Due to The...

The Issue: The battery capacity of the optional PS500 power supply unit for the...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 4, 2016· Abbott Vascular

Recalled Item: MitraClip Clip Delivery System Recalled by Abbott Vascular Due to Abbott...

The Issue: Abbott Vascular has recently received reports of cases on Clip Delivery...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 4, 2016· Bard Peripheral Vascular Inc

Recalled Item: Bard TruGuide Disposable Coaxial Biopsy Needle Product Usage: The TruGuide...

The Issue: Bard Peripheral Vascular, Inc. is recalling Bard TruGuide Disposable Coaxial...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2016· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens Healthcare Diagnostic ADVIA Centaur Calibrator E- 6- Pack ()...

The Issue: ADVIA Centaur Systems Calibrator E Lot 42 and 43 Bias with the Testosterone...

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

Class II — Potential Health HazardOngoing
FoodFebruary 4, 2016· The Sausage Maker, Inc.

Recalled Item: THE SAUSAGE MAKER SEASONING Summer Sausage under the following labels:...

The Issue: Fermento ingredient contains undeclared whey protein and skim milk powder

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 4, 2016· The Sausage Maker, Inc.

Recalled Item: THE SAUSAGE MAKER SEASONING Dried Sausage Sticks under the following...

The Issue: Fermento ingredient contains undeclared whey protein and skim milk powder

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 4, 2016· The Sausage Maker, Inc.

Recalled Item: THE SAUSAGE MAKER SEASONING Trail Bologna under the following labels:...

The Issue: Fermento ingredient contains undeclared whey protein and skim milk powder

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 4, 2016· The Sausage Maker, Inc.

Recalled Item: THE SAUSAGE MAKER SEASONING Goetburg Summer Sausage under the following...

The Issue: Fermento ingredient contains undeclared whey protein and skim milk powder

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 4, 2016· The Sausage Maker, Inc.

Recalled Item: THE SAUSAGE MAKER SEASONING Smoked Pepperoni under the following labels:...

The Issue: Fermento ingredient contains undeclared whey protein and skim milk powder

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

Class I — Serious Health HazardOngoing
Refund