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. 1,129 recalls have been distributed to Kansas in the last 12 months.
Showing 1821–1840 of 28,538 recalls
Recalled Item: Skytron Freedom 4FXS-60 Heavy Duty Monitor Mount Recalled by IHB OPERATIONS...
The Issue: The mounting hardware that is supplied with the 4FXS-60 monitor bracket does...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Introducer Kit- Tearaway MicroSlide Recalled by Galt Medical Corporation Due...
The Issue: Due to a potential open seal in the sterile barrier packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: B Braun Interventional Coaxial Dilator Recalled by Galt Medical Corporation...
The Issue: Due to a potential open seal in the sterile barrier packaging .
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: B Braun Interventional ELITE HV Hemostasis Valve Introducer System by Galt...
The Issue: Due to a potential open seal in the sterile barrier packaging .
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: restor3d Cordera Hip System. ACETABULAR LINER GRP C 36MM LIP. Recalled by...
The Issue: The hip cup liner that was packaged with the incorrect labeling....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IceSeed 1.5 CX S NEEDLE US Recalled by Boston Scientific Corporation Due to...
The Issue: Boston Scientific has identified that IceSeedTM CX needles manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Biomet Ceramic Head Recalled by Zimmer, Inc. Due to The associated...
The Issue: The associated product labeling does not adequately provide compatibility...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IceSeed 1.5 CX S NEEDLE OUS Recalled by Boston Scientific Corporation Due to...
The Issue: Boston Scientific has identified that IceSeedTM CX needles manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IceSeed 1.5 CX NEEDLE OUS Recalled by Boston Scientific Corporation Due to...
The Issue: Boston Scientific has identified that IceSeedTM CX needles manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IceSeed 1.5 CX NEEDLE US Recalled by Boston Scientific Corporation Due to...
The Issue: Boston Scientific has identified that IceSeedTM CX needles manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T Master/Nova Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V....
The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Enterprise 1.5T Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...
The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T Power/Pulsar Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V....
The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T Explorer/Nova Dual Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND...
The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 3.0T Quasar Dual Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V....
The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Biomet Ceramic Head Recalled by Zimmer, Inc. Due to The associated...
The Issue: The associated product labeling does not adequately provide compatibility...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartPath to dStream for 1.5T Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND...
The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T R11 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...
The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to The...
The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.0T Power/Pulsar Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V....
The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.