Product Recalls in Indiana
Product recalls affecting Indiana — including food, drugs, consumer products, medical devices, and vehicles distributed to Indiana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,725 recalls have been distributed to Indiana in the last 12 months.
Showing 9501–9520 of 29,228 recalls
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: 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: 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: 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.
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.
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.
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.