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. 2,517 recalls have been distributed to Michigan in the last 12 months.
Showing 35001–35020 of 53,342 recalls
Recalled Item: Huberts Lemonade Strawberry Recalled by Coca-Cola Company (The) Due to...
The Issue: The product may contain foreign material (glass) in some bottles.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Huberts Lemonade Watermelon Recalled by Coca-Cola Company (The) Due to...
The Issue: The product may contain foreign material (glass) in some bottles.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Raw Cucumbers Recalled by Maglio & Co Ready Fresh Due to Potential...
The Issue: A sample of raw cucumbers tested positive for Salmonella spp.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Zyston¿ Transform Implant Kit. Model Number PCR8200-3101. Device labeled...
The Issue: Zimmer Bioment Spine, Inc. announces a voluntary field action for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medivance ArcticGel Neonatal Pad The pad is designed to fit Recalled by C.R....
The Issue: An internal review of an available product found that the Information For...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Avenir M¿ller Stem 4 Standard Avenir M¿ller Stem 6 Lateral Recalled by...
The Issue: Product mix-up. The Avenir M¿ller Stem 6 lateral uncemented might be placed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zyston¿ Transform Instrument Case. Model Number PCR8200-2101. Device labeled...
The Issue: Zimmer Bioment Spine, Inc. announces a voluntary field action for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TAZORAC (tazarotene) Gel 0.05% Recalled by Allergan Sales, LLC Due to Failed...
The Issue: Failed Content Uniformity Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Glipizide 2.5 mg Extended-release tablets Recalled by Actavis Inc Due to...
The Issue: Failed Dissolution Specifications: Glipizide 2.5 mg ER Tablets exceeded...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TAZORAC (tazarotene) Gel 0.05% Recalled by Allergan Sales, LLC Due to Failed...
The Issue: Failed Content Uniformity Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Methylprednisolone Acetate/Lidocaine HCl 40/10 mg/mL Injection Recalled by...
The Issue: Lack of Processing Controls: Isomeric Pharmacy Solution, LLC announces a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TRYX Antibacterial Envelope Rx Only Product Usage: Indicated for...
The Issue: TRYX products are being recalled since the processes of spaying, welding,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TransMotion Medical Recalled by Winco Mfg., LLC Due to Non-conforming...
The Issue: Non-conforming component caused arms of TMM4 Stretcher chair to no longer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TransMotion Medical Recalled by Winco Mfg., LLC Due to Non-conforming...
The Issue: Non-conforming component caused arms of TMM4 Stretcher chair to no longer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TransMotion Medical Recalled by Winco Mfg., LLC Due to Non-conforming...
The Issue: Non-conforming component caused arms of TMM4 Stretcher chair to no longer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureStep Tray Recalled by C.R. Bard, Inc. Due to Labeling problem
The Issue: Labeling problem
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ArjoHuntleigh Sara Combilizer Recalled by ARJOHUNTLEIGH POLSKA Sp. z.o.o....
The Issue: ArjoHuntleigh has concluded that a device tipping hazard may occur on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRYX Neuro Absorbable Antibacterial Envelope Product Usage: Indicated for...
The Issue: TRYX products are being recalled since the processes of spaying, welding,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRYX Absorbable Antibacterial Envelope Product Usage: Indicated for...
The Issue: TRYX products are being recalled since the processes of spaying, welding,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spirit Plus Bed Recalled by CHG Hospital Beds Inc Due to Stryker Medical is...
The Issue: Stryker Medical is initiating a voluntary recall of the Spirit Select and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.