Product Recalls in Kansas
Product recalls affecting Kansas — including food, drugs, consumer products, medical devices, and vehicles distributed to Kansas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,341 recalls have been distributed to Kansas in the last 12 months.
Showing 43601–43620 of 50,117 recalls
Recalled Item: Endo Illuminator Recalled by Synergetics Inc Due to Faulty seals on the...
The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: "The Corona" Shielded Wide Field Endo Illuminator Recalled by Synergetics...
The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 25ga Awh Chandelier Recalled by Synergetics Inc Due to Faulty seals on the...
The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance iCT & Brilliance iCT SP Computed Tomography X-Ray Systems...
The Issue: Patient images exhibited ring artifacts.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 25ga Mid-Field Endo Illuminator Recalled by Synergetics Inc Due to Faulty...
The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vivid (tm) Endo Illuminator Recalled by Synergetics Inc Due to Faulty seals...
The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 25ga Awh Chandelier Recalled by Synergetics Inc Due to Faulty seals on the...
The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 23ga Endo Illuminator (Eckardt Trocar Compatible) Recalled by Synergetics...
The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Standard tubing set Recalled by Synergetics Inc Due to Faulty seals on the...
The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 25ga Wide Field Corona Endo Illuminator Recalled by Synergetics Inc Due to...
The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 23ga Wide Field Corona Endo Illuminator Recalled by Synergetics Inc Due to...
The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BACTEC FX- Top Unit instrument Recalled by Becton Dickinson & Co. Due to...
The Issue: Improperly functioning component of a diagnostic medical device may cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 23ga Wide Field Endo Illuminator Recalled by Synergetics Inc Due to Faulty...
The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 27ga ONE-STEP (tm) Awh/Tano Vivid Chandelier Recalled by Synergetics Inc Due...
The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stiff 25ga Endo Illuminator Recalled by Synergetics Inc Due to Faulty seals...
The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wide Field Endo Illuminator Recalled by Synergetics Inc Due to Faulty seals...
The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 29ga Oshima Dual Chandelier Recalled by Synergetics Inc Due to Faulty seals...
The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arthrocare SPORTS MEDICINE Recalled by ArthroCare Medical Corporation Due to...
The Issue: A sharp edge on the cannulated tip of the device may damage or cut a suture.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FOLIC ACID INJECTION Recalled by Fresenius Kabi USA, LLC Due to Failed...
The Issue: Failed Impurities/Degradation specifications: out-of-specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Heartware HVAD Pump Implant Kit (Heartware Ventricular Assist Device)...
The Issue: The housing to the Pump's driveline connector became partially or fully...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.