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. 1,059 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
1,059 in last 12 months

Showing 14281–14300 of 28,538 recalls

Medical DeviceMarch 25, 2019· Change Healthcare Israel Ltd.

Recalled Item: McKesson Cardiology Hemo Recalled by Change Healthcare Israel Ltd. Due to...

The Issue: users are not notified of procedure medication discrepancies between the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2019· Canon Medical System, USA, INC.

Recalled Item: Canon Aquilion Prime SP Recalled by Canon Medical System, USA, INC. Due to...

The Issue: Scanning may be interrupted due to an error during execution of the eXam...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2019· Canon Medical System, USA, INC.

Recalled Item: Canon Aquilion One Recalled by Canon Medical System, USA, INC. Due to...

The Issue: Scanning may be interrupted due to an error during execution of the eXam...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2019· Canon Medical System, USA, INC.

Recalled Item: Canon Aquilion One Vision Recalled by Canon Medical System, USA, INC. Due to...

The Issue: Scanning may be interrupted due to an error during execution of the eXam...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2019· Canon Medical System, USA, INC.

Recalled Item: Canon Aquilion One Recalled by Canon Medical System, USA, INC. Due to...

The Issue: Scanning may be interrupted due to an error during execution of the eXam...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2019· Canon Medical System, USA, INC.

Recalled Item: Canon Aquilion Precision Recalled by Canon Medical System, USA, INC. Due to...

The Issue: Scanning may be interrupted due to an error during execution of the eXam...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2019· Canon Medical System, USA, INC.

Recalled Item: Canon Aquilion Lightning Recalled by Canon Medical System, USA, INC. Due to...

The Issue: Scanning may be interrupted due to an error during execution of the eXam...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2019· Canon Medical System, USA, INC.

Recalled Item: Canon Aquilion Prime Recalled by Canon Medical System, USA, INC. Due to...

The Issue: Scanning may be interrupted due to an error during execution of the eXam...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2019· Canon Medical System, USA, INC.

Recalled Item: Canon Aquilion Premium Recalled by Canon Medical System, USA, INC. Due to...

The Issue: Scanning may be interrupted due to an error during execution of the eXam...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2019· Stryker Communications

Recalled Item: Berchtold Chromophare F528 Surgical Lights. Product Usage: The medical...

The Issue: The back cover of the light head was insufficiently assembled and could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2019· Cardinal Health 200, LLC

Recalled Item: ChemoPlus Chemo Spill Kit Product Code:CT4004 Product Usage: ChemoPlus...

The Issue: Kit label states not made with natural rubber latex,however safety goggles...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: Cios Alpha with software version VA30-mobile C-arm x-ray Material # Recalled...

The Issue: Continuous operation of the Cios Alpha at high tube outputs may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2019· Cardinal Health 200, LLC

Recalled Item: ChemoPlus Chemo Spill Kit Recalled by Cardinal Health 200, LLC Due to Kit...

The Issue: Kit label states not made with natural rubber latex,however safety goggles...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2019· Cardinal Health 200, LLC

Recalled Item: ChemoPlus Protective Wrap-around Goggles Product Code:DP5030G Product Usage:...

The Issue: Kit label states not made with natural rubber latex,however safety goggles...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2019· Stryker Communications

Recalled Item: Berchtold Chromophare F628 Surgical Lights. Product Usage: The medical...

The Issue: The back cover of the light head was insufficiently assembled and could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2019· Cardinal Health 200, LLC

Recalled Item: ChemoPlus Chemo Spill Kit Product Code:DP5016K Product Usage: ChemoPlus...

The Issue: Kit label states not made with natural rubber latex,however safety goggles...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: syngo.via syngo.CT Cardiac Function Recalled by Siemens Medical Solutions...

The Issue: There is a potential risk of a wrong measurement in the annulus plane during...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: syngo.via syngo.CT Cardiac Planning Recalled by Siemens Medical Solutions...

The Issue: There is a potential risk of a wrong measurement in the annulus plane during...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2019· Edwards Lifesciences, LLC

Recalled Item: EV1000 Clinical Platform Recalled by Edwards Lifesciences, LLC Due to...

The Issue: Potential for an electrical short circuit leading to possible fire hazard...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 21, 2019· Conmed Corporation

Recalled Item: ConMed Anchor Tissue Retrieval System" Recalled by Conmed Corporation Due to...

The Issue: Voids in the seal or a partial seal results in an open channel and may...

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

Class II — Potential Health HazardOngoing