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. 2,632 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,632 in last 12 months

Showing 1928119300 of 53,342 recalls

Medical DeviceMay 7, 2020· Stryker GmbH

Recalled Item: Stryker End Cap T2 Humerus ¿6mm Recalled by Stryker GmbH Due to Seal...

The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2020· Stryker GmbH

Recalled Item: Stryker Locking Screw Recalled by Stryker GmbH Due to Seal integrity of the...

The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2020· Stryker GmbH

Recalled Item: Stryker Locking Screw Recalled by Stryker GmbH Due to Seal integrity of the...

The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2020· Stryker GmbH

Recalled Item: Stryker Locking Screw Recalled by Stryker GmbH Due to Seal integrity of the...

The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2020· Stryker GmbH

Recalled Item: Stryker Locking Screw Recalled by Stryker GmbH Due to Seal integrity of the...

The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2020· Stryker GmbH

Recalled Item: Stryker End Cap Recalled by Stryker GmbH Due to Seal integrity of the...

The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2020· Stryker GmbH

Recalled Item: Stryker Locking Screw Recalled by Stryker GmbH Due to Seal integrity of the...

The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...

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

Class II — Potential Health HazardOngoing
FoodMay 6, 2020· Jindilli Beverages LLC

Recalled Item: Milkadamia Salted Buttery Spread 8 ounces packaged in plastic tub Recalled...

The Issue: Potential to contain mold

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 6, 2020· Jindilli Beverages LLC

Recalled Item: Milkadamia Unsalted Buttery Spread 8 ounces packaged in plastic tub Recalled...

The Issue: Potential to contain mold

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 6, 2020· Endologix, Inc.

Recalled Item: Ovation iX Abdominal Stent Graft Systems Recalled by Endologix, Inc. Due to...

The Issue: A material weakness adjacent to the polymer fill channel may become...

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

Class I — Serious Health HazardOngoing
DrugMay 5, 2020· Exela Pharma Sciences LLC

Recalled Item: Potassium Acetate Injection Recalled by Exela Pharma Sciences LLC Due to...

The Issue: Short Fill

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

Class III — Low RiskOngoing
Refund
DrugMay 5, 2020· Mylan Institutional LLC

Recalled Item: Aloprim (allopurinol sodium) for Injection Recalled by Mylan Institutional...

The Issue: Discoloration: Out-of-specification results for appearance obtained during...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 5, 2020· Olympus Corporation of the Americas

Recalled Item: ENF-GP2 Rhino-Laryngo Fiberscope - Product Usage: is indicated for use...

The Issue: Products repaired with the incorrect service manual may be missing an O ring...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2020· Zimmer Biomet, Inc.

Recalled Item: Vital MIS Spinal Fixation system implants CANN POLY EXT TAB 5.5X35MM...

The Issue: There are reports of inadequate locking of the extended tab screws....

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2020· Zimmer Biomet, Inc.

Recalled Item: Vital MIS Spinal Fixation system implants CANN POLY EXT TAB 4.5X45MM...

The Issue: There are reports of inadequate locking of the extended tab screws....

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2020· Zimmer Biomet, Inc.

Recalled Item: Vital MIS Spinal Fixation system implants CANN BL POLY EXT 8.5X55MM Recalled...

The Issue: There are reports of inadequate locking of the extended tab screws....

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2020· Zimmer Biomet, Inc.

Recalled Item: Vital MIS Spinal Fixation system implants CANN POLY EXT TAB 5.5X50MM...

The Issue: There are reports of inadequate locking of the extended tab screws....

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2020· Zimmer Biomet, Inc.

Recalled Item: Vital MIS Spinal Fixation system implants CANN POLY EXT TAB 5.5X45MM...

The Issue: There are reports of inadequate locking of the extended tab screws....

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2020· Zimmer Biomet, Inc.

Recalled Item: Vital MIS Spinal Fixation system implants CANN BL POLY EXT 8.5X60MM Recalled...

The Issue: There are reports of inadequate locking of the extended tab screws....

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2020· Zimmer Biomet, Inc.

Recalled Item: Vital MIS Spinal Fixation system implants CANN POLY EXT TAB 6.5X40MM...

The Issue: There are reports of inadequate locking of the extended tab screws....

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

Class II — Potential Health HazardOngoing