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. 976 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
976 in last 12 months

Showing 35881–35900 of 50,117 recalls

Medical DeviceNovember 20, 2015· Bigwall Enterprises

Recalled Item: WARM STEAM Personal Steam Inhaler-Adjustable control to regulate flow of...

The Issue: "The public reason for the recall is that the product is being recalled out...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2015· Biomet, Inc.

Recalled Item: A.L.P.S. 4.0mm Cancellous Locking Screws intended for use in stabilization...

The Issue: These screws have a single lead (instead of a triple lead) thread. The screw...

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

Class II — Potential Health HazardOngoing
FoodNovember 20, 2015· Made In Nature, LLC

Recalled Item: Made In Nature Sriracha Chili Kale Chips Recalled by Made In Nature, LLC Due...

The Issue: Made in Nature is recalling Made In Nature Sriracha Chili Kale Chips and...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodNovember 20, 2015· Made In Nature, LLC

Recalled Item: Pacific Superfoods Snack Lava Rock Sriracha Kale Chips Recalled by Made In...

The Issue: Made in Nature is recalling Made In Nature Sriracha Chili Kale Chips and...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 19, 2015· Biomerieux

Recalled Item: Etest¿ PIP/TAZO/CON-4 PTC 256 -pack of 30 tests US. Etest¿ Recalled by...

The Issue: Due to the potential for reporting erroneous results for...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 19, 2015· Biomerieux

Recalled Item: Etest¿ PIP/TAZO/CON-4 PTC 256 - Foam of 100 tests US. Recalled by Biomerieux...

The Issue: Due to the potential for reporting erroneous results for...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 19, 2015· Biomerieux

Recalled Item: Etest¿ PIP/TAZO/CON-4 PTC 256 - Foam of 100 tests WW. Recalled by Biomerieux...

The Issue: Due to the potential for reporting erroneous results for...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 19, 2015· Boston Scientific Corporation

Recalled Item: Boston Scientific Recalled by Boston Scientific Corporation Due to Boston...

The Issue: Boston Scientific is voluntarily recalling its Chariot" Guiding Sheath. To...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 19, 2015· Biomerieux

Recalled Item: Etest¿ Piperacillin/tazobactam (4 ug/mL) PTc0.016-256-pack of 30 tests WW...

The Issue: Due to the potential for reporting erroneous results for...

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

Class I — Serious Health HazardOngoing
DrugNovember 19, 2015· Teva Pharmaceuticals USA

Recalled Item: NABUMETONE Tablets USP Recalled by Teva Pharmaceuticals USA Due to Labeling:...

The Issue: Labeling: Not Elsewhere Classified: Lack of leaflets and approved labels on...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceNovember 18, 2015· Rainbow Specialty & Health Products

Recalled Item: Dressit-X Recalled by Rainbow Specialty & Health Products Due to Rainbow...

The Issue: Rainbow Specialty & Health Products initiated a field action for Dressol-X...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2015· Cyberonics, Inc

Recalled Item: Cyberonics Vagus Nerve Stimulator VNS Therapy AspireSR Generator Recalled by...

The Issue: Certain Model 106 Pulse Generators demonstrate delays in sensing during use...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2015· Radiometer America Inc

Recalled Item: TCM CombiM Modules 903-111 Recalled by Radiometer America Inc Due to...

The Issue: Radiometer America, Inc. is recalling TCM CombiM on rare occasions they may...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: Software version VD10E for Syngo X-Workplace Recalled by Siemens Medical...

The Issue: Potential post-processing software issue when using tabcard "4D" on...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2015· Mevion Medical Systems, Inc.

Recalled Item: MEVION S250 Radiation therapy system Recalled by Mevion Medical Systems,...

The Issue: The treatment table positioning belt can slip gear positions, resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2015· Rainbow Specialty & Health Products

Recalled Item: Dressol-X Recalled by Rainbow Specialty & Health Products Due to Rainbow...

The Issue: Rainbow Specialty & Health Products initiated a field action for Dressol-X...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2015· Olympus Corporation of the Americas

Recalled Item: Olympus ENDOEYE HD II Video Telescopes. Models WA50040A ENDOEYE HD II...

The Issue: A damaged temperature sensor at the ENDOEYE tip caused the distal end to...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2015· Biomet, Inc.

Recalled Item: Biomet Integral Centralizer Hip System Recalled by Biomet, Inc. Due to PMMA...

The Issue: PMMA is listed as a material on the label but the product does not contain PMMA.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo Imaging XS is a Picture Archiving and Communication System (PACS)...

The Issue: For the Syngo Workflow SLR System with Software Ver: VB10C: Printouts may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2015· Owens & Minor Distribution, Inc.

Recalled Item: MediChoice Cohesive Bandages Recalled by Owens & Minor Distribution, Inc....

The Issue: MediChoice sterile cohesive bandages imported and sold under a private brand...

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

Class II — Potential Health HazardOngoing