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. 1,893 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
1,893 in last 12 months

Showing 2004120060 of 28,538 recalls

Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: T100-022WF Recalled by WalkMed Infusion, LLC Due to WalkMed Infusion, LLC...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: T095-022 Recalled by WalkMed Infusion, LLC Due to WalkMed Infusion, LLC...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: T095-120 IV Set with 1.2 Micron Filter. Packaged in a Tyvek pouch Recalled...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: T090-022V 90" 20 Drop IV Admin Set Needle free Y-Site Recalled by WalkMed...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: T100-000F Recalled by WalkMed Infusion, LLC Due to WalkMed Infusion, LLC...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: Spike Set Recalled by WalkMed Infusion, LLC Due to WalkMed Infusion, LLC...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: T100-022F with 0.22 micron filter and FP Clip. Packaged in a Tyvek pouch...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: The pump (with cushioning foam inserts) is packaged in a Recalled by WalkMed...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of the Triton...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: T030-000 -30" 20 Drop IV Admin Secondary Set. Packaged in a Tyvek pouch...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: T100-000VF Recalled by WalkMed Infusion, LLC Due to WalkMed Infusion, LLC...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2016· Cardiovascular Systems Inc

Recalled Item: ViperWire Advance Peripheral Guide Wire Recalled by Cardiovascular Systems...

The Issue: The pouch label was missing the use by date (UBD) of 2018-04.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2016· Dako North America Inc.

Recalled Item: Dako HER2 CISH pharmDx Kit Recalled by Dako North America Inc. Due to An...

The Issue: An incorrect HER2 probe concentration was used when producing the probe...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2016· Biomet, Inc.

Recalled Item: TSP Hip Fracture Plating System device Recalled by Biomet, Inc. Due to...

The Issue: The screw may fracture at the junction of the shaft and the head during...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2016· Heartware, Inc.

Recalled Item: HeartWare Ventricular Assist System Controller Product Usage: For use as...

The Issue: Loose connector ports in controller body.

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 8, 2016· Terumo Cardiovascular Systems Corporation

Recalled Item: HX2" Temperature Management Systems Recalled by Terumo Cardiovascular...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) is conducting a voluntary recall...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2016· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: Peripherally Inserted Central Catheters (PICC) Recalled by Angiodynamics...

The Issue: There is a potential for stylet stiffening that is not accurately...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2016· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns TCM Recalled by Terumo Cardiovascular Systems Corporation Due to...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) is conducting a voluntary recall...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2016· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: Peripherally Inserted Central Catheters (PICC) Recalled by Angiodynamics...

The Issue: There is a potential for stylet stiffening that is not accurately...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2016· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns TCM II Recalled by Terumo Cardiovascular Systems Corporation Due to...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) is conducting a voluntary recall...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2016· Terumo Cardiovascular Systems Corporation

Recalled Item: Preamendments device-Sarns Dual Cooler-Heater. The Sarns Dual Cooler-Heater...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) is conducting a voluntary recall...

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

Class II — Potential Health HazardOngoing