Product Recalls in Mississippi

Product recalls affecting Mississippi — including food, drugs, consumer products, medical devices, and vehicles distributed to Mississippi. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,571 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,571 in last 12 months

Showing 1508115100 of 49,744 recalls

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· 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 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· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Models with SW version VD12 listed below: Artis zee Recalled by...

The Issue: Due to a software error, the IAS (Image Acquisition System) may sporadically...

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· 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· BAXTER HEALTHCARE CORPORATION

Recalled Item: Sharesource Connectivity Platform for Use with the Amia Automated PD System...

The Issue: Baxter Healthcare Corporation has identified that the AMIA Sharesource User...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2021· BAXTER HEALTHCARE CORPORATION

Recalled Item: Kaguya Automated Peritoneal Dialysis System Recalled by BAXTER HEALTHCARE...

The Issue: Baxter Healthcare Corporation has identified that the AMIA Sharesource User...

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

Class II — Potential Health HazardOngoing
DrugJune 29, 2021· Eli Lilly & Company

Recalled Item: Zyprexa Intramuscular Recalled by Eli Lilly & Company Due to cGMP...

The Issue: cGMP deviations: Atypical appearance, decrease in size and change in color...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
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 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 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 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