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 39761–39780 of 53,342 recalls
Recalled Item: - Wild River Pacific Smoked Salmon 4oz. D-Cut Products are Recalled by The...
The Issue: The Santa Barbara Smokehouse, Inc. is recalling fresh and frozen cold smoked...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cambridge House Royal Smoked Salmon Sliced Side Products are packaged...
The Issue: The Santa Barbara Smokehouse, Inc. is recalling fresh and frozen cold smoked...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: - Cambridge House River Run Royal Smoked Salmon Products are Recalled by The...
The Issue: The Santa Barbara Smokehouse, Inc. is recalling fresh and frozen cold smoked...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: - Cambridge House Mild Smoked Salmon Sliced Side - Grade Recalled by The...
The Issue: The Santa Barbara Smokehouse, Inc. is recalling fresh and frozen cold smoked...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Lutera (0.1 mg levonorgestrel and 0.02 mg ethinyl estradiol tablets USP)...
The Issue: Labeling: Incorrect or Missing Package Insert; Product is being recalled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dr Blue Pain Relieving Gel Recalled by Indiana Botanic Gardens, Inc Due to...
The Issue: Superpotent Drug: Product may not be uniformly blended resulting in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rifampin for Injection Recalled by Fresenius Kabi USA, LLC Due to Failed...
The Issue: Failed Impurities/Degradation Specifications; out-of-specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Panoramic X-ray Model PC-1000 The PC-1000 will enable the user Recalled by...
The Issue: Jackscrew nut part failure potentially leading to device malfunction and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew BIRMINGHAM HIP (TM) RESURFACING FEMORAL HEAD Recalled by...
The Issue: The firm observed that the BIRMINGHAM HIP(TM) Resurfacing (BHR) System had...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew BIRMINGHAM HIP (TM) RESURFACING ACETABULAR CUP W/IMPACTOR...
The Issue: The firm observed that the BIRMINGHAM HIP(TM) Resurfacing (BHR) System had...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew BIRMINGHAM HIP (TM) RESURFACING DYSPLASIA CUP W/IMPACTOR...
The Issue: The firm observed that the BIRMINGHAM HIP(TM) Resurfacing (BHR) System had...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smart Lipo Dietary Supplement capsules Recalled by Centro Naturista Due to...
The Issue: Marketed without an approved NDA/ANDA - Product contains undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Smart Lipo Dietary Supplement capsules Recalled by Centro Naturista Due to...
The Issue: Marketed without an approved NDA/ANDA - Product contains undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SERFAS 90 degree Energy Probe Recalled by Stryker Endoscopy Due to Stryker...
The Issue: Stryker Endoscopy is recalling all non expired SERFAS 90 degree Energy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Medley LVP Frame Membrane. Intended use to hold platen Recalled by...
The Issue: Administration of inappropriate quantities of fluid can result, with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Medley LVP Bezel Assembly. Intended use to hold platen Recalled by...
The Issue: Administration of inappropriate quantities of fluid can result, with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perkin Elmer WIZARD2 10-detector Recalled by Perkinelmer Due to Error in...
The Issue: Error in WIZARD2 Barcode ID Label #023 Content may produce erroneous results
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perkin Elmer WIZARD2 1-detector Recalled by Perkinelmer Due to Error in...
The Issue: Error in WIZARD2 Barcode ID Label #023 Content may produce erroneous results
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perkin Elmer WIZARD2 5-detector Recalled by Perkinelmer Due to Error in...
The Issue: Error in WIZARD2 Barcode ID Label #023 Content may produce erroneous results
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perkin Elmer WIZARD2 1-detector Recalled by Perkinelmer Due to Error in...
The Issue: Error in WIZARD2 Barcode ID Label #023 Content may produce erroneous results
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.