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. 2,707 recalls have been distributed to Michigan in the last 12 months.
Showing 7081–7100 of 53,342 recalls
Recalled Item: Synapse PACS - Version 7.3.000 Recalled by FUJIFILM Healthcare Americas...
The Issue: Measurements on a Secondary Capture 2D image, that does not have pixel...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synapse PACS - Version 7.2.200 Recalled by FUJIFILM Healthcare Americas...
The Issue: Measurements on a Secondary Capture 2D image, that does not have pixel...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirLife Adult Manual Resuscitator Recalled by Vyaire Medical Due to Risk of...
The Issue: Risk of hypoventilation caused by duckbill and ring broken/disassembled, due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirLife Adult Manual Resuscitator Recalled by Vyaire Medical Due to Risk of...
The Issue: Risk of hypoventilation caused by duckbill and ring broken/disassembled, due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirLife Adult Manual Resuscitator Recalled by Vyaire Medical Due to Risk of...
The Issue: Risk of hypoventilation caused by duckbill and ring broken/disassembled, due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirLife Adult Manual Resuscitator Recalled by Vyaire Medical Due to Risk of...
The Issue: Risk of hypoventilation caused by duckbill and ring broken/disassembled, due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirLife Adult Manual Resuscitator Recalled by Vyaire Medical Due to Risk of...
The Issue: Risk of hypoventilation caused by duckbill and ring broken/disassembled, due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirLife Adult Manual Resuscitator Recalled by Vyaire Medical Due to Risk of...
The Issue: Risk of hypoventilation caused by duckbill and ring broken/disassembled, due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirLife Adult Manual Resuscitator Recalled by Vyaire Medical Due to Risk of...
The Issue: Risk of hypoventilation caused by duckbill and ring broken/disassembled, due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirLife Adult Manual Resuscitator Recalled by Vyaire Medical Due to Risk of...
The Issue: Risk of hypoventilation caused by duckbill and ring broken/disassembled, due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirLife Adult Manual Resuscitator Recalled by Vyaire Medical Due to Risk of...
The Issue: Risk of hypoventilation caused by duckbill and ring broken/disassembled, due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Signature Laparoscopic Instruments Recalled by Silex Medical, LLC Due to...
The Issue: Insulation on the tube did not extend fully to the proximal end of the shaft...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Signature Laparoscopic Instruments Recalled by Silex Medical, LLC Due to...
The Issue: Insulation on the tube did not extend fully to the proximal end of the shaft...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Signature Laparoscopic Instruments Recalled by Silex Medical, LLC Due to...
The Issue: Insulation on the tube did not extend fully to the proximal end of the shaft...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Signature Laparoscopic Instruments Recalled by Silex Medical, LLC Due to...
The Issue: Insulation on the tube did not extend fully to the proximal end of the shaft...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Signature Laparoscopic Instruments Recalled by Silex Medical, LLC Due to...
The Issue: Insulation on the tube did not extend fully to the proximal end of the shaft...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Signature Laparoscopic Instruments Recalled by Silex Medical, LLC Due to...
The Issue: Insulation on the tube did not extend fully to the proximal end of the shaft...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Signature Laparoscopic Instruments Recalled by Silex Medical, LLC Due to...
The Issue: Insulation on the tube did not extend fully to the proximal end of the shaft...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Signature Laparoscopic Instruments Recalled by Silex Medical, LLC Due to...
The Issue: Insulation on the tube did not extend fully to the proximal end of the shaft...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custodiol HTK Solution Recalled by Dr Franz Koehler Chemie Gmbh Due to...
The Issue: Potential for particles to be present in solution.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.