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 3806138080 of 53,342 recalls

DrugNovember 11, 2015· RemedyRepack Inc.

Recalled Item: Novolin 70/30 Recalled by RemedyRepack Inc. Due to Labeling: Incorrect...

The Issue: Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 11, 2015· RemedyRepack Inc.

Recalled Item: Humulin 70/30 Recalled by RemedyRepack Inc. Due to Labeling: Incorrect...

The Issue: Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 11, 2015· Fagron, Inc

Recalled Item: SyrSpend SF Recalled by Fagron, Inc Due to Microbial Contamination of...

The Issue: Microbial Contamination of Non-Sterile Products: Syrspend SF and Syrspend SF...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 11, 2015· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Acute Care CCRP CalPak-in vitro diagnostic product intended to...

The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2015· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Acute Care CTNI TestPak-in vitro diagnostic test for the Recalled by...

The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2015· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Acute Care MYO DilPak Catalog Number: CMYO-D SMN:10445081 in...

The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2015· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Acute Care" MYO TestPak-in vitro diagnostic test for the Recalled by...

The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2015· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Acute Care CKMB DilPak- an in vitro diagnostic product Recalled by...

The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2015· ConvaTec, Inc

Recalled Item: Nebulizer Masks Opti-Mist and Opti-Mist Clear Nebulizer masks are intended...

The Issue: The Nebulizer mask malfunctions in that there is reduced or no aerosol...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2015· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Acute Care BHCG CalPak-in vitro diagnostic product intended to...

The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2015· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Acute Care BHCG TestPak-an in vitro diagnostic product intended...

The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2015· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Acute Care DDMR TestPak Catalog Number: CDDMRE SMN: 10701511...

The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2015· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Acute Care" CCRP TestPak-in vitro diagnostic product intended to...

The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2015· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Acute Care CKMB TestPak- in vitro diagnostic test for Recalled by...

The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2015· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Acute Care pBNP TestPak- in vitro diagnostic test for Recalled by...

The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2015· C.R. Bard, Inc.

Recalled Item: Arctic Sun 5000 and Arctic Sun 2000 Recalled by C.R. Bard, Inc. Due to...

The Issue: Improper targeted temperature therapy was delivered to patients because the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2015· Zimmer, Inc.

Recalled Item: Zimmer UNIVERSAL Power System Loaner and Modular Electric/Battery Single...

The Issue: The firm identified a malfunction which made it possible for a handpiece to...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2015· Aesculap, Inc.

Recalled Item: Tray Set containing multiple instruments and may contain the flexible bone...

The Issue: The flexible shaft of the instruments may break during orthopedic spinal...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2015· OrthoPediatrics Corp

Recalled Item: UniAxial Pedicle Screw & UniAxial Reduction Pedicle Screw The Response...

The Issue: Response Spine UniAxial Pedicle & UniAxial Reduction Pedicle Screws may have...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2015· Zimmer, Inc.

Recalled Item: Zimmer UNIVERSAL Power System Loaner and Modular Electric/Battery Double...

The Issue: The firm identified a malfunction which made it possible for a handpiece to...

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

Class II — Potential Health HazardOngoing