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. 1,813 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
1,813 in last 12 months

Showing 3476134780 of 53,342 recalls

FoodJuly 25, 2016· Let's Do Lunch, Inc.

Recalled Item: Chicken Double Dogs on Whole Grain Bun Product ID 809021 Recalled by Let's...

The Issue: Potential Listeria monocytogenes contamination.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 25, 2016· Microgenics Corporation

Recalled Item: DRI Salicylate Serum Tox Assay Recalled by Microgenics Corporation Due to...

The Issue: Some lots of DRI Salicylate Serum Tox Assay negative patient samples are...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2016· Terumo Cardiovascular Systems Corp

Recalled Item: Terumo Custom Cardiovascular System Cardiovascular Procedure Kits labeled...

The Issue: Terumo Custom Cardiovascular Procedure Kits are labeled as Xcoating surface...

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

Class II — Potential Health HazardOngoing
FoodJuly 23, 2016· Arcobasso Foods

Recalled Item: Panera Bread Balsamic Vinaigrette Dressing Recalled by Arcobasso Foods Due...

The Issue: Consumer complaints of bulging bottles.

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

Class III — Low RiskOngoing
Refund
Medical DeviceJuly 22, 2016· GE OEC Medical Systems, Inc

Recalled Item: OEC UroView 2800 Recalled by GE OEC Medical Systems, Inc Due to A firmware...

The Issue: A firmware issue in the supplied LCD workstation monitor(s). Under some...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2016· GE OEC Medical Systems, Inc

Recalled Item: OEC 9800 Recalled by GE OEC Medical Systems, Inc Due to A firmware issue in...

The Issue: A firmware issue in the supplied LCD workstation monitor(s). Under some...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2016· Inovo, Inc

Recalled Item: INOVO Purefill Oxygen Compressor Model PF1100 Is an oxygen Recalled by...

The Issue: Device can fail during operation.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2016· Smith & Nephew, Inc.

Recalled Item: RENASYS Sterile Transparent Film and all the RENASYS Dressing kits Recalled...

The Issue: Sterility seal integrity failures on the Renasys Sterile Transparent Film

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2016· Integra LifeSciences Corp.

Recalled Item: Large QWIX Compression screw Recalled by Integra LifeSciences Corp. Due to...

The Issue: Labeling on the Qwix Screw product states that it is a "compression screw"...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2016· Zimmer Biomet, Inc.

Recalled Item: ROSA Brain 3.0.0 Usage: The device is intended for the Recalled by Zimmer...

The Issue: Communication errors between ROSANNA BRAIN software, MARIO software and the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2016· Sterling Diagnostics, Inc.

Recalled Item: Sterling Diagnostics Recalled by Sterling Diagnostics, Inc. Due to Sterling...

The Issue: Sterling Diagnostics, Inc. initiated a recall on 7/20/2016 for multiple...

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

Class III — Low RiskOngoing
Medical DeviceJuly 20, 2016· Sterling Diagnostics, Inc.

Recalled Item: Urea Nitrogen/Color BUN (Enzymatic Berthelot) for IN VITRO DIAGNOSTIC USE...

The Issue: Sterling Diagnostics, Inc. initiated a recall on 7/20/2016 for multiple...

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

Class III — Low RiskOngoing
Medical DeviceJuly 20, 2016· Sterling Diagnostics, Inc.

Recalled Item: Enzymatic Cholesterol (Trinder/COD-CEH) for IN VITRO DIAGNOSTIC USE in the...

The Issue: Sterling Diagnostics, Inc. initiated a recall on 7/20/2016 for multiple...

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

Class III — Low RiskOngoing
Medical DeviceJuly 20, 2016· Sterling Diagnostics, Inc.

Recalled Item: Sterling Diagnostics Recalled by Sterling Diagnostics, Inc. Due to Sterling...

The Issue: Sterling Diagnostics, Inc. initiated a recall on 7/20/2016 for multiple...

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

Class III — Low RiskOngoing
Medical DeviceJuly 20, 2016· Sterling Diagnostics, Inc.

Recalled Item: Sterling Diagnostics Recalled by Sterling Diagnostics, Inc. Due to Sterling...

The Issue: Sterling Diagnostics, Inc. initiated a recall on 7/20/2016 for multiple...

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

Class III — Low RiskOngoing
Medical DeviceJuly 20, 2016· Sterling Diagnostics, Inc.

Recalled Item: Creatinine/Endpoint [Modified Heinegard-Tiderstrom] for IN VITRO DIAGNOSTIC...

The Issue: Sterling Diagnostics, Inc. initiated a recall on 7/20/2016 for multiple...

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

Class III — Low RiskOngoing
Medical DeviceJuly 20, 2016· Sterling Diagnostics, Inc.

Recalled Item: Sterling Diagnostics Recalled by Sterling Diagnostics, Inc. Due to Sterling...

The Issue: Sterling Diagnostics, Inc. initiated a recall on 7/20/2016 for multiple...

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

Class III — Low RiskOngoing
Medical DeviceJuly 20, 2016· Sterling Diagnostics, Inc.

Recalled Item: Sterling Diagnostics Recalled by Sterling Diagnostics, Inc. Due to Sterling...

The Issue: Sterling Diagnostics, Inc. initiated a recall on 7/20/2016 for multiple...

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

Class III — Low RiskOngoing
Medical DeviceJuly 20, 2016· Sterling Diagnostics, Inc.

Recalled Item: Sterling Diagnostics Recalled by Sterling Diagnostics, Inc. Due to Sterling...

The Issue: Sterling Diagnostics, Inc. initiated a recall on 7/20/2016 for multiple...

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

Class III — Low RiskOngoing
Medical DeviceJuly 20, 2016· Cardinal Health

Recalled Item: BLUE IMPERVIOUS GOWN WITH THUMBHOOKS Recalled by Cardinal Health Due to Blue...

The Issue: Blue Impervious Gown with thumbhooks, X-large. All lots do not meet design...

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

Class II — Potential Health HazardOngoing