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. 2,692 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,692 in last 12 months

Showing 1094110960 of 53,342 recalls

DrugDecember 6, 2022· Camber Pharmaceuticals, Inc

Recalled Item: Lacosamide Oral Solution Recalled by Camber Pharmaceuticals, Inc Due to...

The Issue: Failed Excipient Specifications: out of specification result observed for...

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

Class III — Low RiskOngoing
Refund
Medical DeviceDecember 6, 2022· Zimmer, Inc.

Recalled Item: NexGen Option Stemmed Tibial Component Size 7 Recalled by Zimmer, Inc. Due...

The Issue: Zimmer Biomet is conducting a voluntary medical device recall related to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2022· Zimmer, Inc.

Recalled Item: NexGen Option Stemmed Tibial Component Size 5 Recalled by Zimmer, Inc. Due...

The Issue: Zimmer Biomet is conducting a voluntary medical device recall related to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2022· Zimmer, Inc.

Recalled Item: NexGen Option Stemmed Tibial Component Size 4 Recalled by Zimmer, Inc. Due...

The Issue: Zimmer Biomet is conducting a voluntary medical device recall related to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2022· Zimmer, Inc.

Recalled Item: NexGen Option Stemmed Tibial Component Size 6 Recalled by Zimmer, Inc. Due...

The Issue: Zimmer Biomet is conducting a voluntary medical device recall related to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2022· Zimmer, Inc.

Recalled Item: NexGen Option Stemmed Tibial Component Size 8 Recalled by Zimmer, Inc. Due...

The Issue: Zimmer Biomet is conducting a voluntary medical device recall related to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2022· Zimmer, Inc.

Recalled Item: NexGen Option Stemmed Tibial Component Size 3 Recalled by Zimmer, Inc. Due...

The Issue: Zimmer Biomet is conducting a voluntary medical device recall related to the...

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

Class II — Potential Health HazardOngoing
DrugDecember 5, 2022· RemedyRepack Inc.

Recalled Item: Desmopressin Acetate Tablet Recalled by RemedyRepack Inc. Due to Subpotent...

The Issue: Subpotent Drug: repackaged product was recalled by the manufacturer for...

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 5, 2022· Northern Food I/E Inc.

Recalled Item: Beijing Hawthorne Candy Recalled by Northern Food I/E Inc. Due to Undeclared...

The Issue: Product contains undeclared sulfites (7.32 mg/serving)

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 5, 2022· Cranberry Sweets & More Inc

Recalled Item: Recalled Meltaways product is packaged in clear cellophane bags Recalled by...

The Issue: Peanut Butter Meltaway was mis-labeled as Mint Meltaways and peanut is...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceDecember 5, 2022· Turbett Surgical, Inc.

Recalled Item: Turbett Surgical Container Recalled by Turbett Surgical, Inc. Due to Pod may...

The Issue: Pod may have weld failures breaching the sterile barrier and result in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2022· Turbett Surgical, Inc.

Recalled Item: Turbett Surgical Container Recalled by Turbett Surgical, Inc. Due to Pod may...

The Issue: Pod may have weld failures breaching the sterile barrier and result in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2022· Align Technology Inc

Recalled Item: Invisalign Express 10 Invisalign System Comprehensive Recalled by Align...

The Issue: 3D orthodontic planning software has a defect that leads to an issue where...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2022· Cardiac Assist, Inc

Recalled Item: SHIP KIT Recalled by Cardiac Assist, Inc Due to A software update (v1.1.5)...

The Issue: A software update (v1.1.5) has been developed to address the issue of...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 5, 2022· Young Dental Manufacturing I, LLC

Recalled Item: Denticator PICK-A-DENT Recalled by Young Dental Manufacturing I, LLC Due to...

The Issue: mislabeled product

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

Class III — Low RiskOngoing
Medical DeviceDecember 5, 2022· Elekta, Inc.

Recalled Item: Oncentra Brachy radiation therapy planning system software. Recalled by...

The Issue: A reconstruction error may occur when using the Catheter Bending...

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

Class II — Potential Health HazardOngoing
DrugDecember 2, 2022· GlaxoSmithKline Consumer Healthcare Holdings LLC

Recalled Item: TUMS Antacid Recalled by GlaxoSmithKline Consumer Healthcare Holdings LLC...

The Issue: Presence of Foreign Substance: The foreign material is primarily comprised...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 2, 2022· GlaxoSmithKline Consumer Healthcare Holdings LLC

Recalled Item: TUMS Antacid Recalled by GlaxoSmithKline Consumer Healthcare Holdings LLC...

The Issue: Presence of Foreign Substance: The foreign material is primarily comprised...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 2, 2022· GlaxoSmithKline Consumer Healthcare Holdings LLC

Recalled Item: TUMS Antacid Recalled by GlaxoSmithKline Consumer Healthcare Holdings LLC...

The Issue: Presence of Foreign Substance: The foreign material is primarily comprised...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 2, 2022· GlaxoSmithKline Consumer Healthcare Holdings LLC

Recalled Item: TUMS Antacid Recalled by GlaxoSmithKline Consumer Healthcare Holdings LLC...

The Issue: Presence of Foreign Substance: The foreign material is primarily comprised...

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

Class II — Potential Health HazardOngoing
Refund