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. 2,434 recalls have been distributed to Michigan in the last 12 months.
Showing 1301–1320 of 29,286 recalls
Recalled Item: BritePro Solo Mini Single-Use Fiber Optic Laryngoscope Handle Recalled by...
The Issue: Laryngoscope handles may not illuminate as intended.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELEOS SEGMENTAL LIMB SALVAGE SYSTEM Recalled by Onkos Surgical, Inc. Due to...
The Issue: Unidentified substance of unknown impact was identified on devices during a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELEOS SEGMENTAL LIMB SALVAGE SYSTEM Recalled by Onkos Surgical, Inc. Due to...
The Issue: Unidentified substance of unknown impact was identified on devices during a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELEOS SEGMENTAL LIMB SALVAGE SYSTEM Recalled by Onkos Surgical, Inc. Due to...
The Issue: Unidentified substance of unknown impact was identified on devices during a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Description/ PYXIS MEDBANK MINI 1FH-1FM/169-137 Recalled by CareFusion 303,...
The Issue: Reports of delayed access to medication in automated dispensing cabinets...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access Thyroglobulin assay Recalled by Beckman Coulter, Inc. Due to Access...
The Issue: Access Thyroglobulin reagent lot 439163 may generate erroneously high...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multi Joystick R-net. Electrical wheelchair component. Recalled by mo-Vis...
The Issue: Devices with firmware versions 2.3 and lower may experience timing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IDM-ARLITE-R. Electrical wheelchair component. Recalled by mo-Vis BVBA Due...
The Issue: Devices with firmware versions 2.3 and lower may experience timing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Micro Joystick R-net. Electrical wheelchair component. Recalled by mo-Vis...
The Issue: Devices with firmware versions 2.3 and lower may experience timing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IDM-MICRO-R. Electrical wheelchair component. Recalled by mo-Vis BVBA Due to...
The Issue: Devices with firmware versions 2.3 and lower may experience timing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IDM-MULTI-R. Electrical wheelchair component. Recalled by mo-Vis BVBA Due to...
The Issue: Devices with firmware versions 2.3 and lower may experience timing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FilmArray NGDS Warrior Panel NGDS-ASY-0007 is a qualitative Recalled by...
The Issue: FilmArray NGDS Warrior Panel (NGDS-ASY-0007) has an increased risk of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: All-round Joystick R-net Light. Electrical wheelchair component. Recalled by...
The Issue: Devices with firmware versions 2.3 and lower may experience timing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microbore Extension Set with 0.2 Micron Filter. Catalog Number: V6215....
The Issue: Label is incorrect. The product label indicates that the device contains an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: EMPOWR 3D KNEE TIBIAL INSERT - E-PLUS Product Recalled by Encore...
The Issue: Knee implants contain incorrect labeling (size and/or side incorrect)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: EMPOWR 3D KNEE TIBIAL INSERT - E-PLUS Product Recalled by Encore...
The Issue: Knee implants contain incorrect labeling (size and/or side incorrect)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products Ca Slides Recalled by Ortho-Clinical Diagnostics,...
The Issue: Generations 67 and above of VITROS Ca Slides are experiencing an increased...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ambu SPUR II Labeled as the following: 1 SPUR II Adult Resuscitator Recalled...
The Issue: Potential for the manometer port being blocked rendering the manometer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Medline General Surgery Tray is customized to meet requirements Recalled...
The Issue: Affected kits contain recalled Stryker Color Cuff Sterile Disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Trucount Controls Recalled by Becton, Dickinson and Company, BD Bio...
The Issue: Control kits contain incorrect standard deviation (SD) values for the low...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.