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. 1,933 recalls have been distributed to Kansas in the last 12 months.
Showing 15961–15980 of 28,538 recalls
Recalled Item: Proteus 235 Recalled by Ion Beam Applications S.A. Due to Correction vector...
The Issue: Correction vector confirmation message is lost if access point is changed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD FACS Universal Loader (Optional) to the BD FACSLyric Clinical System...
The Issue: The solenoid plunger tip length is too short resulting in insufficient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Recalled by Abbott Laboratories, Inc Due to An update to the Reagents...
The Issue: An update to the Reagents and Specimen Collection and Handling/Preparation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Immunoglobulin A is an in vitro diagnostic assay for the Recalled by Abbott...
The Issue: An update to the Reagents and Specimen Collection and Handling/Preparation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Immunoglobulin G is an in vitro diagnostic assay for the Recalled by Abbott...
The Issue: An update to the Reagents and Specimen Collection and Handling/Preparation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C3 is an in vitro diagnostic assay for the quantitative Recalled by Abbott...
The Issue: An update to the Reagents and Specimen Collection and Handling/Preparation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Draeger Jaundice Meter JM-103 The device is intended for use in hospitals...
The Issue: Users have misinterpreted the display for out of range measurement indicated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MegaPower Electrosurgical Generator Recalled by Megadyne Medical Products,...
The Issue: If two devices are plugged into the same channel/port in the generator, both...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAREstream ProNox Nitrous Oxide Delivery System labeled as the following:...
The Issue: Two analgesic gas delivery system oxygen/nitrous oxide mixers were reported...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Draeger Jaundice Meter JM-105 The device is intended for use in hospitals...
The Issue: Users have misinterpreted the display for out of range measurement indicated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Safety Sideport Knife 1.0mm 45¿ Recalled by Beaver Visitec Due to Blades are...
The Issue: Blades are loose in handles and may fall out due to non cured epoxy
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Minicon Clinical Sample Concentrators for In Vitro Diagnostic Use 9031...
The Issue: In vitro diagnostic devices, used greater than 6 months after date of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AdvanDx QuickFISH Slides Recalled by Opgen Inc Due to Possible diminished...
The Issue: Possible diminished performance prior to its established expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanguard Knee System PS Tibial Bearing Recalled by Zimmer Biomet, Inc. Due...
The Issue: The label master file was errantly set up as a 63/37mm instead of a 63/67mm....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus JF-160F duodenoscopes (Model NumberJF-160F) Recalled by Olympus...
The Issue: Issuance of validated, new reprocessing procedures. The new cleaning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus JF-140F duodenoscopes (Model NumberJF-140F) Recalled by Olympus...
The Issue: Issuance of validated, new reprocessing procedures. This corrective action...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bio-Stable 5F DL-55CM IR-145 Kit Non-Valved PG Recalled by Angiodynamics...
The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RS - TANDEM 5F DL BIOFLO MIDLINE Recalled by Angiodynamics Inc. (Navilyst...
The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RS TANDEM 5F DL BIOFLO PASV Recalled by Angiodynamics Inc. (Navilyst Medical...
The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bio-Stable 5F SL-55CM IR-145 Kit Valved PG Recalled by Angiodynamics Inc....
The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.