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. 1,030 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
1,030 in last 12 months

Showing 14621–14640 of 47,632 recalls

Medical DeviceJune 30, 2021· Olympus Corporation of the Americas

Recalled Item: Soltive Premium Super Pulsed Laser System (TFL-PLS) & Pro Super Recalled by...

The Issue: Thermal injury following dusting and fragmenting treatment of ureteral...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2021· GE Healthcare, LLC

Recalled Item: Computed Tomography Systems Revolution CT Recalled by GE Healthcare, LLC Due...

The Issue: The accumulated dose is incorrectly displayed in certain situations....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2021· GE Healthcare, LLC

Recalled Item: Revolution Apex Recalled by GE Healthcare, LLC Due to The accumulated dose...

The Issue: The accumulated dose is incorrectly displayed in certain situations. There...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2021· Hitachi Healthcare Americas Corporation

Recalled Item: Model L43K Intraoperative Probe-For the diagnostic ultrasound evaluation...

The Issue: The screw cover at the tip of the probe may fall off after a cleaning and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2021· GE Healthcare, LLC

Recalled Item: Revolution CT Recalled by GE Healthcare, LLC Due to The accumulated dose is...

The Issue: The accumulated dose is incorrectly displayed in certain situations. There...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2021· Exactech, Inc.

Recalled Item: Exactech Connexion GXL acetabular polyethylene liners used in the following...

The Issue: Risk of edge-loading and premature prosthesis wear is possible in a specific...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2021· Exactech, Inc.

Recalled Item: Exactech Connexion GXL acetabular polyethylene liners used in the following...

The Issue: Risk of edge-loading and premature prosthesis wear is possible in a specific...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2021· Oakworks Inc

Recalled Item: Vascular Table without Fowler (USV1) and Ultrasound Vascular Table with...

The Issue: Weld failure- the bracket attaches the tabletop tilting actuator to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2021· Exactech, Inc.

Recalled Item: Exactech Connexion GXL acetabular polyethylene liners used in the following...

The Issue: Risk of edge-loading and premature prosthesis wear is possible in a specific...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2021· Exactech, Inc.

Recalled Item: Exactech Connexion GXL acetabular polyethylene liners used in the following...

The Issue: Risk of edge-loading and premature prosthesis wear is possible in a specific...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2021· Exactech, Inc.

Recalled Item: Exactech BIOLOX delta Femoral Head Recalled by Exactech, Inc. Due to Biolox...

The Issue: Biolox Delta Femoral Head was packaged and labeled as 170-36-00 (36mm +0),...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2021· Exactech, Inc.

Recalled Item: Exactech Connexion GXL acetabular polyethylene liners used in the following...

The Issue: Risk of edge-loading and premature prosthesis wear is possible in a specific...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2021· Exactech, Inc.

Recalled Item: Exactech Connexion GXL acetabular polyethylene liners used in the following...

The Issue: Risk of edge-loading and premature prosthesis wear is possible in a specific...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2021· Exactech, Inc.

Recalled Item: Exactech Connexion GXL acetabular polyethylene liners used in the following...

The Issue: Risk of edge-loading and premature prosthesis wear is possible in a specific...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2021· Exactech, Inc.

Recalled Item: Exactech Connexion GXL acetabular polyethylene liners used in the following...

The Issue: Risk of edge-loading and premature prosthesis wear is possible in a specific...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2021· Exactech, Inc.

Recalled Item: Exactech Connexion GXL acetabular polyethylene liners used in the following...

The Issue: Risk of edge-loading and premature prosthesis wear is possible in a specific...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2021· Exactech, Inc.

Recalled Item: Exactech Connexion GXL acetabular polyethylene liners used in the following...

The Issue: Risk of edge-loading and premature prosthesis wear is possible in a specific...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2021· Exactech, Inc.

Recalled Item: Exactech Connexion GXL acetabular polyethylene liners used in the following...

The Issue: Risk of edge-loading and premature prosthesis wear is possible in a specific...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2021· Exactech, Inc.

Recalled Item: Exactech BIOLOX delta Femoral Head Recalled by Exactech, Inc. Due to Biolox...

The Issue: Biolox Delta Femoral Head was packaged and labeled as 170-36-00 (36mm +0),...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2021· Exactech, Inc.

Recalled Item: Exactech Connexion GXL acetabular polyethylene liners used in the following...

The Issue: Risk of edge-loading and premature prosthesis wear is possible in a specific...

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

Class II — Potential Health HazardOngoing