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. 2,492 recalls have been distributed to Michigan in the last 12 months.
Showing 38561–38580 of 53,342 recalls
Recalled Item: Baby Omega 3 Dietary supplement (in liquid form) Recalled by Zarbee's...
The Issue: Some units of each lot may contain contaminants (elevated aerobic plate...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Baby Vitamin D Dietary supplement (in liquid form) Recalled by Zarbee's...
The Issue: Some units of each lot may contain contaminants (elevated aerobic plate...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: TheraSphere(R) YTTRIUM-90 CLASS MICROSPHERE INJECTION TheraSphere¿ is...
The Issue: One mislabeled dose of TheraSphere¿ Y-90 Glass Microspheres, which was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Valeant Pharmaceuticals North America Recalled by Valeant Pharmacueticals...
The Issue: The Serial I.D. Label and some information in the Operation Manual for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOMET 3i Recalled by Biomet 3i, LLC Due to Inadequate biocompatibility testing.
The Issue: Inadequate biocompatibility testing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOMET 3i Recalled by Biomet 3i, LLC Due to Inadequate biocompatibility testing.
The Issue: Inadequate biocompatibility testing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOMET 3i Recalled by Biomet 3i, LLC Due to Inadequate biocompatibility testing.
The Issue: Inadequate biocompatibility testing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOMET 3i Recalled by Biomet 3i, LLC Due to Inadequate biocompatibility testing.
The Issue: Inadequate biocompatibility testing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthopaedics Duracon Flat Tibial Wedge Cemented use only Sterile....
The Issue: Stryker Orthopaedics has received two customer complaints regarding Duracon...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Digital Lightbox Recalled by Brainlab AG Due to Potentially incorrectly...
The Issue: Potentially incorrectly displayed objects when actively deselecting a fused...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Screw Inserter Recalled by Synthes (USA) Products LLC Due to Certain...
The Issue: Certain lots of the Screw Inserter may be etched with incorrect graphics....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4FR Single Lumen Pressure Injectable PICC Recalled by Arrow International...
The Issue: Labeling inaccuracy in the Instructions for Use (IFU) and Patient Card. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WellPatch¿ Capsaicin Pain Relief Patch Recalled by The Mentholatum Co. Due...
The Issue: Labeling: Incorrect Instructions; The word not is missing from the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: UN1002 Air Recalled by Praxair Inc. Due to CGMP Deviations: Confirmed...
The Issue: CGMP Deviations: Confirmed customer compliant of odor when turning on a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: UN1002 Air Recalled by Praxair Inc. Due to CGMP Deviations: Confirmed...
The Issue: CGMP Deviations: Confirmed customer compliant of odor when turning on a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nabulsi Cheese 16 oz Recalled by Karoun Dairies Due to Potential Listeria...
The Issue: Karoun Dairies is recalling all cheese manufactured from an identified...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Mozzarella Natural Hickory Smoked Net Wt. 1lb. Codes: 7 96252 70012 5...
The Issue: Karoun Dairies is recalling all cheese manufactured from an identified...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Goat Milk Feta 8 oz Codes: 7 96252 50001 Recalled by Karoun Dairies Due to...
The Issue: Karoun Dairies is recalling all cheese manufactured from an identified...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Authentic Braided String Cheese Jumbo Braided String Cheese Braided Whole...
The Issue: Karoun Dairies is recalling all cheese manufactured from an identified...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cotija 8 oz Recalled by Karoun Dairies Due to Potential Listeria Contamination
The Issue: Karoun Dairies is recalling all cheese manufactured from an identified...
Recommended Action: Do not consume. Return to store for a refund or discard.