Product Recalls in Missouri
Product recalls affecting Missouri — including food, drugs, consumer products, medical devices, and vehicles distributed to Missouri. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,648 recalls have been distributed to Missouri in the last 12 months.
Showing 9501–9520 of 29,298 recalls
Recalled Item: ACCESS SARS-CoV-2 ANTIGEN QC Recalled by Beckman Coulter Inc. Due to...
The Issue: SARS-CoV-2 Antigen Assay test may generate false positive results which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Triathlon Prim CEM FXD BPLT 7 Recalled by Howmedica Osteonics Corp. Due to...
The Issue: The internal profile of the Triathlon Prim (Baseplate) is potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GlideScope Go Monitors Recalled by Verathon, Inc. Due to Handheld video...
The Issue: Handheld video monitor failed to meet the labeled IP67 rating which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access SARS-CoV-2 Antigen Calibrators Recalled by Beckman Coulter Inc. Due...
The Issue: SARS-CoV-2 Antigen Assay test may generate false positive results which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.