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. 2,742 recalls have been distributed to Michigan in the last 12 months.
Showing 2201–2220 of 29,286 recalls
Recalled Item: MEDITECH Expanse Laboratory (LAB) Recalled by Medical Information...
The Issue: Entering multiple keys that trigger input simultaneously may remove data...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DxI 9000 Access Immunoassay Analyzer Recalled by Beckman Coulter, Inc. Due...
The Issue: the DxI 9000 encoder wheel was misaligned on the motor shaft, leading to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access 2 Immunoassay Analyzer Recalled by Beckman Coulter, Inc. Due to...
The Issue: Beckman Coulter identified that an issue for Access 2 Sample Motors (B48016)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aortic Root Cannula: 1. DLP Aortic Root Cannula A. CANNULA Recalled by...
The Issue: Unexpected loose material in the male luer used in the aortic root cannula...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rotarex Atherectomy System and Instructions for Use Recalled by Bard...
The Issue: Atherectomy Catheter eIFU updated to clarify and emphasize procedural steps...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Sigma Spectrum Infusion System (V6 Platform) Recalled by Baxter...
The Issue: There is the potential for missing motor mounting screws, which may have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Spectrum IQ Infusion System with Dose IQ Safety Software Recalled by...
The Issue: There is the potential for missing motor mounting screws, which may have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelePACS (Image Fusion Module) - InteleViewer Recalled by INTELERAD...
The Issue: A software application that receives digital images and data from various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CRANI PACK Recalled by American Contract Systems Inc Due to During an...
The Issue: During an internal investigation, ACS was unable to confirm that the CODMAN...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IsoLoc Short Profile Prostate Immobilization Treatment Balloon Device Kit...
The Issue: Product is mislabeled with the incorrect fill volume.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HemosIL LMW Heparin Controls Recalled by Instrumentation Laboratory Due to...
The Issue: Multiple complaints indicating lower than expected quality control (QC)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioMEMS Heart Failure (HF) System that consist of: -CardioMEMS Hospital...
The Issue: Due to issues associated with data migration of patient information and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: TBS Osteo Product Name: TBS iNsight Model/Catalog Number:...
The Issue: Potential variability in calculations from fast array scans compared to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access Erythropoietin (EPO) Recalled by Beckman Coulter, Inc. Due to...
The Issue: Affected lot (439363) exhibited a negative dose drop of -22% with native...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Numerous models of nonsterile hemostatic forceps: (1) Recalled by Aesculap...
The Issue: The forceps have been used in ways not covered by the design resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Numerous models of nonsterile hemostatic forceps: (1) Recalled by Aesculap...
The Issue: The forceps have been used in ways not covered by the design resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Numerous models of nonsterile hemostatic forceps: (1) Recalled by Aesculap...
The Issue: The forceps have been used in ways not covered by the design resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Numerous models of nonsterile hemostatic forceps: (1) Recalled by Aesculap...
The Issue: The forceps have been used in ways not covered by the design resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Numerous models of nonsterile hemostatic forceps: (1) Recalled by Aesculap...
The Issue: The forceps have been used in ways not covered by the design resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniMed insulin pump Recalled by Medtronic MiniMed, Inc. Due to All...
The Issue: All Medtronic MiniMed pumps (Paradigm series, Minimed 530G, 6XX series, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.