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. 1,893 recalls have been distributed to Kansas in the last 12 months.
Showing 19201–19220 of 28,538 recalls
Recalled Item: HF Cable WA00014A Recalled by Olympus Corporation of the Americas Due to...
The Issue: Software malfunction that results in incorrect generation or display of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has become...
The Issue: GE Healthcare has become aware of a potential safety issue where certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition Edge Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: Siemens is releasing a software update that provides bug-fixes to improve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition AS Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Siemens is releasing a software update that provides bug-fixes to improve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition Flash Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: Siemens is releasing a software update that provides bug-fixes to improve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q Recalled by Siemens Medical Solutions USA, Inc Due to The...
The Issue: The possibility exists that the semi-automatic focus switch may not work as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris System PC unit Recalled by CareFusion 303, Inc. Due to Reports where...
The Issue: Reports where the Low Battery alarm and/or the Very Low Battery alarm are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee/zeego Recalled by Siemens Medical Solutions USA, Inc Due to The...
The Issue: The possibility exists that the semi-automatic focus switch may not work as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM Artis Recalled by Siemens Medical Solutions USA, Inc Due to The...
The Issue: The possibility exists that the semi-automatic focus switch may not work as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes 0.76 mm Drill Bit/Stryker J-Latch/with 5mm Stop/44.5 mm Non-Sterile...
The Issue: Package may be incorrectly labeled as containing 0.76 mm Drill Bit, but in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medi Choice Arm Slings ASL 2103 Small 7.5 x 12.5 Inch 1/EA Recalled by Owens...
The Issue: Owens & Minor is the initial importer and private label distributor of Medi...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Turbo Elite Atherectomy Catheter. Models: 410-152 Recalled by Spectranetics...
The Issue: Spectranetics Corporation announces a voluntary field action for the Turbo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEVION S250 Product Usage: Proton Radiation Therapy Recalled by Mevion...
The Issue: Completing Setup Without Program Move Complete Can Cause An Isocenter Error
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Flexible Shaft Recalled by Synthes (USA) Products LLC Due to...
The Issue: Non-conforming material used.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELCA Coronary Atherectomy Catheter. Models: 110-001 Recalled by...
The Issue: Spectranetics Corporation announces a voluntary field action for the Turbo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bridge Occlusion Balloon. Model: 590-001 Temporary vessel occlusion of the...
The Issue: Spectranetics Corporation announces a voluntary field action for the Turbo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perceval Sutureless Aortic Heart Valve size S Recalled by Sorin Group USA,...
The Issue: Sorin Group USA, Inc. announces a voluntary field action for the Perceval...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MSS CASSETTE GLU/LAC/UREA (BUN) as a part of the Roche Recalled by Roche...
The Issue: Incorrect Urea results may be generated sporadically on cobas b 221<6>Roche...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gomco Circumcision Clamps with separate O-Ring Component: The device is...
The Issue: Aesculap has received complaints of excessive bleeding after use of Gomco...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natus neoBLUE blanket LED Phototherapy system Recalled by Natus Medical...
The Issue: neoBLUE blanket LED Phototherapy System distributed since release of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.