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. 2,428 recalls have been distributed to Michigan in the last 12 months.
Showing 47561–47580 of 53,342 recalls
Recalled Item: P.F. Chang's Home Menu Recalled by Conagra Inc Due to Undeclared Allergens
The Issue: The firm is recalling Pork & Leek Dumplings because Shrimp & Pollack Fish...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Individual units labeled in part: Recalled by Richard Wolf Medical...
The Issue: Richard Wolf Medical Instrument Corporation recieved a complaint stating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERRAD 100NX Cassettes The STERRAD Sterilization System is a low Recalled...
The Issue: Advanced Sterilization Products (ASP) is recalling the three lots (13F049,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Brivo OEC715/785/865 C-Arm Recalled by GE Healthcare Beijing , Hangwei...
The Issue: GE is recalling certain lots of GE Brivo OEC715/785/865 C-Arm due to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERRAD 200 Sterilizer (Single Door) Recalled by Advanced Sterilization...
The Issue: Advanced Sterilization Products (ASP) is recalling the STERRAD 200...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amlodipine Besylate Tablets Recalled by Mylan Institutional, Inc. (d.b.a....
The Issue: CGMP Deviations: Pharmaceuticals were produced and distributed with active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amlodipine Besylate Tablets Recalled by Mylan Institutional, Inc. (d.b.a....
The Issue: CGMP Deviations: Pharmaceuticals were produced and distributed with active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amlodipine Besylate Tablets Recalled by Mylan Institutional, Inc. (d.b.a....
The Issue: CGMP Deviations: Pharmaceuticals were produced and distributed with active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Quinapril Tablets USP Recalled by Lupin Pharmaceuticals Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: During stability testing an...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Quinapril Tablets USP Recalled by Lupin Pharmaceuticals Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: During stability testing an...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Prolia (denosumab) Injection Recalled by Amgen, Inc. Due to Presence of...
The Issue: Presence of Particulate Matter: Visible cellulose fibers were observed in a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Siemens Dimension LOCI TNI Troponin I Calibrator RC 621. The Recalled by...
The Issue: Siemens Dimension LOCI TNI Troponin I calibrator lot 3DD007 may demonstrate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aquarius (TM) TEMPERATURE THERAPY Recalled by DeRoyal Industries Inc Due to...
The Issue: The unit displays an error code of hose kinking when no hose kink is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal (R) Aquarius Hot/Cold Therapy Combo Unit Recalled by DeRoyal...
The Issue: The unit displays an error code of hose kinking when no hose kink is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal (R) Aquarius Hot/Cold Therapy Combo Unit Recalled by DeRoyal...
The Issue: The unit displays an error code of hose kinking when no hose kink is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal (R) Aquarius Hot/Cold Therapy Combo Unit Recalled by DeRoyal...
The Issue: The unit displays an error code of hose kinking when no hose kink is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal (R) Aquarius Hot/Cold Therapy Combo Unit Recalled by DeRoyal...
The Issue: The unit displays an error code of hose kinking when no hose kink is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal (R) Aquarius Hot/Cold Therapy Combo Unit Recalled by DeRoyal...
The Issue: The unit displays an error code of hose kinking when no hose kink is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1% Lidocaine HCl Injection Recalled by Hospira, Inc. Due to Presence of...
The Issue: Presence of Particulate Matter: Oxidized stainless steel found in vial of 1%...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Morphine Sulfate Injection Recalled by Hospira, Inc. Due to Lack of...
The Issue: Lack of Assurance of Sterility: Confirmed customer report of leakage of vial...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.