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. 2,598 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
2,598 in last 12 months

Showing 81018120 of 28,538 recalls

Medical DeviceMay 13, 2022· Covidien, LP

Recalled Item: EEA Autosuture Circular Stapler with DST Series Technology Recalled by...

The Issue: The affected staplers have the potential for the staple guide to not be...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2022· Volcano Corp

Recalled Item: Volcano Visions PV. 035 Digital IVUS Catheter Recalled by Volcano Corp Due...

The Issue: Digital IVUS catheter instructions for use ( IFU) do not contain...

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

Class III — Low RiskOngoing
Medical DeviceMay 13, 2022· Volcano Corp

Recalled Item: Volcano Visions PV. 035 Digital IVUS Catheter Recalled by Volcano Corp Due...

The Issue: Digital IVUS catheter instructions for use ( IFU) do not contain...

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

Class III — Low RiskOngoing
Medical DeviceMay 11, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Pill Splitters Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...

The Issue: Product lid (which houses a blade) is coming unhinged from the base, thus...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2022· GE Healthcare, LLC

Recalled Item: CARESCAPE Central Station (CSCS) V2 Recalled by GE Healthcare, LLC Due to...

The Issue: The CARESAPE Central Station (CSCS) V2 can shut down due to a potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2022· Becton Dickinson & Company

Recalled Item: BD Connecta Stopcock Without Extension Tube Catalog No. 394601 (OUS)...

The Issue: May have the potential for leakage at the housing component of the stopcock,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2022· Becton Dickinson & Company

Recalled Item: BD Connecta Stopcock Without Extension Tube Catalog No. 394600 (OUS)...

The Issue: May have the potential for leakage at the housing component of the stopcock,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2022· Becton Dickinson & Company

Recalled Item: Nexiva with Single BD Connecta Stopcock Version (Pink) Catalog No. 383687...

The Issue: May have the potential for leakage at the housing component of the stopcock,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2022· Becton Dickinson & Company

Recalled Item: BD Connecta White 360 Shelf 100Ea Catalog No. 395000 (OUS) Recalled by...

The Issue: May have the potential for leakage at the housing component of the stopcock,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2022· Becton Dickinson & Company

Recalled Item: BD Connecta Stopcock Without Extension Tube Catalog No. 394602 (OUS)...

The Issue: May have the potential for leakage at the housing component of the stopcock,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2022· Becton Dickinson & Company

Recalled Item: Nexiva with Single BD Connecta Stopcock Version (20 Ga Blue) Recalled by...

The Issue: May have the potential for leakage at the housing component of the stopcock,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2022· Becton Dickinson & Company

Recalled Item: BD Connecta" Plus1 360 Blue Blend Catalog No. 394911 (OUS) Recalled by...

The Issue: May have the potential for leakage at the housing component of the stopcock,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2022· Becton Dickinson & Company

Recalled Item: BD Connecta" Plus3 White Blend OEM (sterile Recalled by Becton Dickinson &...

The Issue: May have the potential for leakage at the housing component of the stopcock,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2022· Becton Dickinson & Company

Recalled Item: BD Connecta Stopcock Without Extension Tube Catalog No. 394605 (OUS)...

The Issue: May have the potential for leakage at the housing component of the stopcock,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2022· Becton Dickinson & Company

Recalled Item: BD Connecta 3-Way Stopcocks Catalog No. 394900 (OUS) Recalled by Becton...

The Issue: May have the potential for leakage at the housing component of the stopcock,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2022· Becton Dickinson & Company

Recalled Item: BD Connecta Stopcock with OFF Directed Tap Without Extension Tube Recalled...

The Issue: May have the potential for leakage at the housing component of the stopcock,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2022· Getinge Usa Sales Inc

Recalled Item: VOLISTA StandOP Surgical Light Recalled by Getinge Usa Sales Inc Due to...

The Issue: Paint particles may detach and fall in the operating field. In the worst...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2022· Microbiologics Inc

Recalled Item: KWIK-STIK" plus: Clostridium perfringens Recalled by Microbiologics Inc Due...

The Issue: Labeling error.

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

Class III — Low RiskOngoing
Medical DeviceMay 5, 2022· ARROW INTERNATIONAL Inc.

Recalled Item: Arrow Three-Lumen CVC Recalled by ARROW INTERNATIONAL Inc. Due to Gravity...

The Issue: Gravity flow rates on the affected product lidstock are incorrect.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2022· Medtronic Inc

Recalled Item: HeartWare Battery Recalled by Medtronic Inc Due to Batteries for the HVAD...

The Issue: Batteries for the HVAD system have a weld defect affecting internal...

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

Class I — Serious Health HazardOngoing