Product Recalls in South Dakota

Product recalls affecting South Dakota — including food, drugs, consumer products, medical devices, and vehicles distributed to South Dakota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,512 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,512 in last 12 months

Showing 1016110180 of 27,558 recalls

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· 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· Medline Industries Inc

Recalled Item: S-O303000 CONTROL Recalled by Medline Industries Inc Due to Medline...

The Issue: Medline Industries, Inc. is removing specific lots of STAT-Site¿ Controls...

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

Class III — Low RiskOngoing
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 cmJL 3.5 Model Number: LA6JL35...

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· Northgate Technologies, Inc.

Recalled Item: Steris CO2MPACT Endoscopic Insufflator system Recalled by Northgate...

The Issue: An internal tubing component in the flow path was made with incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2021· Northgate Technologies, Inc.

Recalled Item: ConMed 50L abdominal insufflator Recalled by Northgate Technologies, Inc....

The Issue: An internal tubing component in the flow path was made with incorrect...

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

Class II — Potential Health HazardOngoing