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. 2,576 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,576 in last 12 months

Showing 2212122140 of 53,342 recalls

Medical DeviceJuly 24, 2019· Allergan PLC

Recalled Item: Natrelle and McGhan Silicone-Filled Breast Implants Recalled by Allergan PLC...

The Issue: The action was initiated following notification by the U.S. FDA of their...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 24, 2019· Allergan PLC

Recalled Item: McGhan Croissant-Shaped Tissue Expanders Recalled by Allergan PLC Due to The...

The Issue: The action was initiated following notification by the U.S. FDA of their...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 24, 2019· Allergan PLC

Recalled Item: Natrelle and McGhan Silicone-Filled Breast Implant BioCell Round Moderate...

The Issue: The action was initiated following notification by the U.S. FDA of their...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 24, 2019· Allergan PLC

Recalled Item: Natrelle 133 Tissue Expanders w/Suture Tabs BIOCELL Full Height Variable...

The Issue: The action was initiated following notification by the U.S. FDA of their...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 24, 2019· Allergan PLC

Recalled Item: Natrelle 133 Tissue Expanders (also named style 133 BIOSPAN Tissue Recalled...

The Issue: The action was initiated following notification by the U.S. FDA of their...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 24, 2019· Allergan PLC

Recalled Item: Natrelle 410 Recalled by Allergan PLC Due to The action was initiated...

The Issue: The action was initiated following notification by the U.S. FDA of their...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 24, 2019· Allergan PLC

Recalled Item: Natrelle 510 Recalled by Allergan PLC Due to The action was initiated...

The Issue: The action was initiated following notification by the U.S. FDA of their...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 24, 2019· Allergan PLC

Recalled Item: McGhan BioDIMENSIONAL silicone-Filled Breast Implants Recalled by Allergan...

The Issue: The action was initiated following notification by the U.S. FDA of their...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 24, 2019· Allergan PLC

Recalled Item: RITZ PRINCESS Recalled by Allergan PLC Due to The action was initiated...

The Issue: The action was initiated following notification by the U.S. FDA of their...

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

Class I — Serious Health HazardOngoing
DrugJuly 23, 2019· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Mometasone Furoate Cream USP Recalled by Glenmark Pharmaceuticals Inc., USA...

The Issue: GMP Deviations: Glenmark received complaints stating that mometasone fuorate...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 23, 2019· New Standard Device Inc

Recalled Item: 'n'-Hole Post which is a component of the Revolution External Recalled by...

The Issue: The threads on posts stripping out when tensioned during application process.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: Mammomat Revelation with software version VC10 and Biopsy Option Intended...

The Issue: An error can occur when performing a biopsy using the InSpect function. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2019· Roche Diagnostics Operations, Inc.

Recalled Item: Online TDM Vancomycin Gen.3 (100 tests) Catalog # 06779336190...

The Issue: Inaccurately Low Sample Results

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2019· Roche Diagnostics Operations, Inc.

Recalled Item: Online TDM Vancomycin Gen.3 ( 200 tests) Catalog # 06779344190 Recalled by...

The Issue: Inaccurately Low Sample Results

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2019· Instrumentation Laboratory Co.

Recalled Item: ROTEM ex-tem Rest of the world part No: 503-05 (ROW) Recalled by...

The Issue: Prolonged clotting times

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2019· Instrumentation Laboratory Co.

Recalled Item: ROTEM ex-tem Canada Part No: 503-05-CA Recalled by Instrumentation...

The Issue: Prolonged clotting times

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2019· Instrumentation Laboratory Co.

Recalled Item: ROTEM ex-tem Recalled by Instrumentation Laboratory Co. Due to Prolonged...

The Issue: Prolonged clotting times

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2019· OMNIlife science Inc.

Recalled Item: OMNIlife science Recalled by OMNIlife science Inc. Due to Acetabular liners...

The Issue: Acetabular liners failed the oxidation testing performed prior to release....

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2019· OMNIlife science Inc.

Recalled Item: OMNIlife science Recalled by OMNIlife science Inc. Due to Acetabular liners...

The Issue: Acetabular liners failed the oxidation testing performed prior to release....

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2019· OMNIlife science Inc.

Recalled Item: OMNIlife science Recalled by OMNIlife science Inc. Due to Acetabular liners...

The Issue: Acetabular liners failed the oxidation testing performed prior to release....

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

Class II — Potential Health HazardOngoing