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. 2,632 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,632 in last 12 months

Showing 1710117120 of 53,342 recalls

Medical DeviceJanuary 15, 2021· Biomet, Inc.

Recalled Item: Central Screw 6.5x25mm - Product Usage: used as a sterile Recalled by...

The Issue: Zimmer Biomet is conducting a lot specific medical device recall for the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2021· RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

Recalled Item: CervAlign Anterior Cervical Plate System-Cervalign Recalled by RTI Surgical,...

The Issue: Locking mechanism has been observed to disassociate either intraoperatively...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2021· RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

Recalled Item: CervAlign Anterior Cervical Plate System-Cervalign Recalled by RTI Surgical,...

The Issue: Locking mechanism has been observed to disassociate either intraoperatively...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2021· Medtronic Vascular

Recalled Item: Medtronic 6F Launcher Guide Catheter 100cm EBU 3.75 Model Number: LA6EBU375...

The Issue: Sterility may be compromised due to an unsealed pouch

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2021· RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

Recalled Item: CervAlign Anterior Cervical Plate System-Cervalign Recalled by RTI Surgical,...

The Issue: Locking mechanism has been observed to disassociate either intraoperatively...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2021· Medtronic Vascular

Recalled Item: Medtronic 6F Launcher Guide Catheter 100 cm EBU 3.0 Model Number: LA6EBU30...

The Issue: Sterility may be compromised due to an unsealed pouch

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2021· RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

Recalled Item: CervAlign Anterior Cervical Plate System-Cervalign Recalled by RTI Surgical,...

The Issue: Locking mechanism has been observed to disassociate either intraoperatively...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2021· RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

Recalled Item: CervAlign Anterior Cervical Plate System-Cervalign Recalled by RTI Surgical,...

The Issue: Locking mechanism has been observed to disassociate either intraoperatively...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2021· RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

Recalled Item: CervAlign Anterior Cervical Plate System-Cervalign Recalled by RTI Surgical,...

The Issue: Locking mechanism has been observed to disassociate either intraoperatively...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2021· RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

Recalled Item: CervAlign Anterior Cervical Plate System-Cervalign Recalled by RTI Surgical,...

The Issue: Locking mechanism has been observed to disassociate either intraoperatively...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2021· RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

Recalled Item: CervAlign Anterior Cervical Plate System-Cervalign Recalled by RTI Surgical,...

The Issue: Locking mechanism has been observed to disassociate either intraoperatively...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2021· RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

Recalled Item: CervAlign Anterior Cervical Plate System-Cervalign Recalled by RTI Surgical,...

The Issue: Locking mechanism has been observed to disassociate either intraoperatively...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2021· RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

Recalled Item: CervAlign Anterior Cervical Plate System-Cervalign Recalled by RTI Surgical,...

The Issue: Locking mechanism has been observed to disassociate either intraoperatively...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2021· RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

Recalled Item: CervAlign Anterior Cervical Plate System-Cervalign Recalled by RTI Surgical,...

The Issue: Locking mechanism has been observed to disassociate either intraoperatively...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2021· RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

Recalled Item: CervAlign Anterior Cervical Plate System-Cervalign Recalled by RTI Surgical,...

The Issue: Locking mechanism has been observed to disassociate either intraoperatively...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2021· Qiagen Sciences LLC

Recalled Item: SARS-CoV-2 Antigen Test Recalled by Qiagen Sciences LLC Due to QIAGEN has...

The Issue: QIAGEN has become aware of the potential for false positive results to occur...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2021· Hamilton Co

Recalled Item: HAMILTON HEATER SHAKER Recalled by Hamilton Co Due to There is a risk that...

The Issue: There is a risk that the device can start a fire if flammable liquids...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2021· RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

Recalled Item: CervAlign Anterior Cervical Plate System-Cervalign Recalled by RTI Surgical,...

The Issue: Locking mechanism has been observed to disassociate either intraoperatively...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2021· RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

Recalled Item: CervAlign Anterior Cervical Plate System-Cervalign Recalled by RTI Surgical,...

The Issue: Locking mechanism has been observed to disassociate either intraoperatively...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2021· RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

Recalled Item: CervAlign Anterior Cervical Plate System-Cervalign Recalled by RTI Surgical,...

The Issue: Locking mechanism has been observed to disassociate either intraoperatively...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing