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. 2,498 recalls have been distributed to Michigan in the last 12 months.
Showing 37961–37980 of 53,342 recalls
Recalled Item: Meijer frozen Butternut Squash Ravioli Recalled by Bertagni 1882 Due to...
The Issue: Meijer frozen Butternut Squash Ravioli is recalled because product may...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Bertagni fresh Sweet Butternut Squash Ravioli Recalled by Bertagni 1882 Due...
The Issue: Bertagni fresh Sweet Butternut Squash Ravioli is recalled because the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Merge RadSuite software. The firm name on the label is Merge Healthcare...
The Issue: The values provided from the Pixel Value tool do not appear to be correct,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MediChoice Cohesive Bandages Recalled by Owens & Minor Distribution, Inc....
The Issue: MediChoice sterile cohesive bandages imported and sold under a private brand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MediChoice Cohesive Bandages Recalled by Owens & Minor Distribution, Inc....
The Issue: MediChoice sterile cohesive bandages imported and sold under a private brand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MediChoice Cohesive Bandages Recalled by Owens & Minor Distribution, Inc....
The Issue: MediChoice sterile cohesive bandages imported and sold under a private brand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Integral Centralizer Hip System Recalled by Biomet, Inc. Due to PMMA...
The Issue: PMMA is listed as a material on the label but the product does not contain PMMA.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet is initiating a...
The Issue: Zimmer Biomet is initiating a recall of the Virage Occipital Eyelet, as it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo Imaging XS is a Picture Archiving and Communication System (PACS)...
The Issue: For the Syngo Workflow SLR System with Software Ver: VB10C: Printouts may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer K2 EDTA (K2E) 5.4mg Plus Blood Collection Tubes. Recalled by...
The Issue: Some tubes were manufactured with the stopper not fully inserted into the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus ENDOEYE HD II Video Telescopes. Models WA50040A ENDOEYE HD II...
The Issue: A damaged temperature sensor at the ENDOEYE tip caused the distal end to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BAKERY FRESH GOODNESS Chocolate Brownie NET WT 16 OZ (1 LB) 453 g CONTAINS:...
The Issue: The firm was notified by a consumer of undeclared walnuts in the product.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sodium Chloride Inhalation Solution Recalled by Nephron Pharmaceuticals...
The Issue: Lack of Assurance of Sterility: Internal dye ingress test failure to assure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sodium Chloride Inhalation Solution Recalled by Nephron Pharmaceuticals...
The Issue: Lack of Assurance of Sterility: Internal dye ingress test failure to assure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovaPACS Diagnostic Viewer versions 8.3.7 Recalled by Novarad Corporation...
The Issue: The SUV values that are being calculated in the PET/CT fusion tool are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radiographic Transparency for Certain and External Connection Tapered...
The Issue: Images contained within radiographic transparency ART 1036 are undersized.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIRMINGHAM HIP RESURFACING MODULAR HEAD Recalled by Smith & Nephew, Inc. Due...
The Issue: The 16 devices distributed in the United States were incorrectly labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DrugSmart Cup 10 Recalled by Ameditech Inc Due to Ameditechs Drugs of Abuse...
The Issue: Ameditechs Drugs of Abuse Tests listed above have shown reduced reactivity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 11 Panel Card (OPI 300) w/Adult Recalled by Ameditech Inc Due to Ameditechs...
The Issue: Ameditechs Drugs of Abuse Tests listed above have shown reduced reactivity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ImmuTest Cup 7-panel w/ Adulteration Recalled by Ameditech Inc Due to...
The Issue: Ameditechs Drugs of Abuse Tests listed above have shown reduced reactivity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.