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. 2,573 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
2,573 in last 12 months

Showing 1068110700 of 28,538 recalls

Medical DeviceNovember 18, 2020· Boston Scientific Corporation

Recalled Item: IceSeed" 1.5 Cryoablation Needle Recalled by Boston Scientific Corporation...

The Issue: Complaint trend regarding needle shaft gas leaks.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2020· Boston Scientific Corporation

Recalled Item: IceSeed" Prostate Cryoablation Kit Recalled by Boston Scientific Corporation...

The Issue: Complaint trend regarding needle shaft gas leaks.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2020· Boston Scientific Corporation

Recalled Item: IceRod" 1.5 CX 90¿ Cryoablation Needle¿ Recalled by Boston Scientific...

The Issue: Complaint trend regarding needle shaft gas leaks.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2020· Boston Scientific Corporation

Recalled Item: Five IceSphere" Prostate Cryoablation Kit Recalled by Boston Scientific...

The Issue: Complaint trend regarding needle shaft gas leaks.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2020· Boston Scientific Corporation

Recalled Item: IcePearl" 2.1 CX Cryoablation Needle Recalled by Boston Scientific...

The Issue: Complaint trend regarding needle shaft gas leaks.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2020· Boston Scientific Corporation

Recalled Item: Five IceRod" i-Thaw" Prostate Cryoablation Kit Recalled by Boston Scientific...

The Issue: Complaint trend regarding needle shaft gas leaks.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2020· Boston Scientific Corporation

Recalled Item: IceRod" Prostate Cryoablation Kit Recalled by Boston Scientific Corporation...

The Issue: Complaint trend regarding needle shaft gas leaks.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2020· Shimadzu Medical Systems

Recalled Item: MH-200S Recalled by Shimadzu Medical Systems Due to The firm has identified...

The Issue: The firm has identified a problem with the control software for the celling...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2020· Boston Scientific Corporation

Recalled Item: IceRod" 1.5 PLUS 90¿ Cryoablation Needle Recalled by Boston Scientific...

The Issue: Complaint trend regarding needle shaft gas leaks.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2020· Aesculap Implant Systems LLC

Recalled Item: ENNOVATE MIS REMOVALKEY SHORT Recalled by Aesculap Implant Systems LLC Due...

The Issue: Fracture or breakage of the spinal fixation arm at the downtube instrument...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2020· Boston Scientific Corporation

Recalled Item: Lotus Edge Valve System Recalled by Boston Scientific Corporation Due to...

The Issue: Failure to execute the visual inspection correctly prior to locking the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceNovember 17, 2020· Zimmer Biomet, Inc.

Recalled Item: Polaris 5.5 Spinal System and Polaris 5.5/Cypher Spinal System Recalled by...

The Issue: Zimmer Biomet is conducting a medical device correction to update the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2020· Remote Diagnostic Technologies Ltd.

Recalled Item: Tempus LS - Manual Defibrillator Recalled by Remote Diagnostic Technologies...

The Issue: A software error was detected within software version 1.3.4 for the Tempus...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2020· Boston Scientific Corporation

Recalled Item: Lotus Edge Valve System Recalled by Boston Scientific Corporation Due to...

The Issue: Failure to execute the visual inspection correctly prior to locking the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceNovember 17, 2020· Boston Scientific Corporation

Recalled Item: Lotus Edge Valve System Recalled by Boston Scientific Corporation Due to...

The Issue: Failure to execute the visual inspection correctly prior to locking the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceNovember 17, 2020· Boston Scientific Corporation

Recalled Item: Lotus Edge Valve System Recalled by Boston Scientific Corporation Due to...

The Issue: Failure to execute the visual inspection correctly prior to locking the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceNovember 17, 2020· Boston Scientific Corporation

Recalled Item: Lotus Edge Valve System Recalled by Boston Scientific Corporation Due to...

The Issue: Failure to execute the visual inspection correctly prior to locking the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceNovember 17, 2020· Boston Scientific Corporation

Recalled Item: Lotus Edge Valve System Recalled by Boston Scientific Corporation Due to...

The Issue: Failure to execute the visual inspection correctly prior to locking the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceNovember 16, 2020· Boston Scientific Corporation

Recalled Item: Contour VL Variable Length Ureteral Stent Recalled by Boston Scientific...

The Issue: Trace amounts of metallic debris were found on the stent related to the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 16, 2020· Covidien Llc

Recalled Item: Capnostream 35 Portable Respiratory Monitor Recalled by Covidien Llc Due to...

The Issue: The firm has released software update V01.05.02.16 (also known as V1.5.2) in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing