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. 2,480 recalls have been distributed to Michigan in the last 12 months.
Showing 43101–43120 of 53,342 recalls
Recalled Item: Crate & Barrel 11.5 oz. Monterey Jack Queso Dip Recalled by Riba Foods Inc...
The Issue: Product may contain undeclared wheat.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Arriba! 16 oz. Chili Con Queso-Hot Recalled by Riba Foods Inc Due to...
The Issue: Product may contain undeclared wheat.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Salpica 8 oz. Ballpark Nacho Recalled by Riba Foods Inc Due to Undeclared Wheat
The Issue: Product may contain undeclared wheat.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: The ATTUNE INTUITION Impaction Handle is a re-useable instrument utilized...
The Issue: Complaints have indicated that the ATTUNE INTUITION Impaction Handle lever...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fixed Tibial bearing ATTUNE INTUITION Impactor The ATTUNE INTUITION...
The Issue: ATTUNE INTUITION Impactors (cat. nos. 254401003, 254401004, and 254401006)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CSA Medical truFreeze System Recalled by CSA Medical Due to An increase in...
The Issue: An increase in complaint trending for a loss of audible sound associated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rotating Tibial Platform ATTUNE INTUITION Impactor. The ATTUNE INTUITION...
The Issue: ATTUNE INTUITION Impactors (cat. nos. 254401003, 254401004, and 254401006)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Femoral Impactor ATTUNE INTUITION Impactor. The ATTUNE INTUITION Impactors...
The Issue: ATTUNE INTUITION Impactors (cat. nos. 254401003, 254401004, and 254401006)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Cabinet X-ray systems Recalled by GE Inspection Technologies, LP Due to...
The Issue: GE discovered these cabinet x-ray systems' potential failure to comply with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Nerve Block Component Recalled by Arrow International Inc Due to Arrow...
The Issue: Arrow is recalling certain lots of the Continuous Nerve Block Component,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile powder Vancomycin Hydrochloride for Injection Recalled by Hospira...
The Issue: Correct Labeled Product Mispack: Product tray containing vials was...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Breas Vivo 50 Home Care Ventilator Product Usage: Respiratory Care Recalled...
The Issue: Unintended treatment termination could result from a keypad malfunction in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSSEOTITE Tapered Certain Implant Rx Only Recalled by Biomet 3i, LLC Due to...
The Issue: Endosseous Dental Implants in contact with a residual machine fluid caused...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSSEOTITE Certain 2 Implant Rx only Recalled by Biomet 3i, LLC Due to...
The Issue: Endosseous Dental Implants in contact with a residual machine fluid caused...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3i T3 Non-Platform Switched Tapered Implant Rx Only Recalled by Biomet 3i,...
The Issue: Endosseous Dental Implants in contact with a residual machine fluid caused...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Licox Brain Tissue Oxygen Monitoring Integra Licox Recon Tissue...
The Issue: Due to a complaint, it was determined that multiple lots of Licox catheters...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ROSA Surgical Device 2.5.8 Recalled by Zimmer Biomet, Inc. Due to Potential...
The Issue: Potential failure of a force feedback sensor that may result in continued...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Small Electric Drive (SED) Recalled by Synthes (USA) Products LLC...
The Issue: The device may operate solely in reverse mode, not operate in reverse mode...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS CHEMISTRY PRODUCTS TRIG Slides Recalled by Ortho-Clinical Diagnostics...
The Issue: Potential for biased results using the specific lot of VITROS CHEMISTRY...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Healon EndoCoat Ophthalmic Viscosurgical Device 3% sodium hyaluronate...
The Issue: AMO has received complaints where the finger grip dislodged while depressing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.