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. 2,603 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
2,603 in last 12 months

Showing 64816500 of 28,538 recalls

Medical DeviceMay 10, 2023· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: CRTD DTPA2D1G COBALT XT HF QUAD OUS Recalled by Medtronic Inc., Cardiac...

The Issue: There is a rare potential for reduced- or no-energy output during high...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 10, 2023· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: CRT-D DTBB2Q1 VIVA QUAD S IS4/DF1 INTL Recalled by Medtronic Inc., Cardiac...

The Issue: There is a rare potential for reduced- or no-energy output during high...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 10, 2023· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: CRT-D DTBA2D4 VIVA XT IS1/DF4 INTL Recalled by Medtronic Inc., Cardiac...

The Issue: There is a rare potential for reduced- or no-energy output during high...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 10, 2023· BearCare, Inc.

Recalled Item: Walnut Wearable Smart Thermometer Recalled by BearCare, Inc. Due to There...

The Issue: There have been reports of skin burns to children wearing the device.

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 9, 2023· Qiagen GmbH

Recalled Item: QIAstat-Dx¿ Respiratory SARS-CoV-2 Panel -IVD intended for the detection and...

The Issue: If cartridges of the affected Serial numbers (SNs) are used, in most cases,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2023· Virtual Radiologic Corp.

Recalled Item: vRad PACS with Mammography Recalled by Virtual Radiologic Corp. Due to The...

The Issue: The error resulted in intermittent failure of current (primary) radiology...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2023· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products Calibrator Kit 20-in vitro diagnostic use only....

The Issue: Potential to cause biased results in the upper end of the reportable range...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2023· Galt Medical Corporation

Recalled Item: Tearaway Introducer Kit Recalled by Galt Medical Corporation Due to Sheath...

The Issue: Sheath introducer assemblies could potentially, due to improper storage...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2023· Remote Diagnostic Technologies Ltd.

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

The Issue: Defibrillator/pacemaker module (DPM) may encounter a problem causing...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2023· Galt Medical Corporation

Recalled Item: Tearaway Introducer Set Recalled by Galt Medical Corporation Due to Sheath...

The Issue: Sheath introducer assemblies could potentially, due to improper storage...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2023· Vyaire Medical

Recalled Item: bellavista 1000e Ventilator Recalled by Vyaire Medical Due to Vyaire Medical...

The Issue: Vyaire Medical identified two patient safety risks during the use of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2023· Vyaire Medical

Recalled Item: bellavista 1000 Ventilator Recalled by Vyaire Medical Due to Vyaire Medical...

The Issue: Vyaire Medical identified two patient safety risks during the use of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2023· T.A.G. MEDICAL PRODUCTS CORPORATION, LTD.

Recalled Item: Betta Link LG Reusable Fishmouth Guide-Intended for use in soft Recalled by...

The Issue: Drill guides might bend when axial forces are applied by surgeon during...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2023· T.A.G. MEDICAL PRODUCTS CORPORATION, LTD.

Recalled Item: BETTA LINK SR REUSABLE PRONGED GUIDE- Intended for use in Recalled by T.A.G....

The Issue: Drill guides might bend when axial forces are applied by surgeon during...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2023· T.A.G. MEDICAL PRODUCTS CORPORATION, LTD.

Recalled Item: BETTA LINK LG KNOTLESS IMPLANT KIT-Intended for use in soft Recalled by...

The Issue: Drill guides might bend when axial forces are applied by surgeon during...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2023· T.A.G. MEDICAL PRODUCTS CORPORATION, LTD.

Recalled Item: Betta Link LG Reusable ProngED Guide - Intended for use Recalled by T.A.G....

The Issue: Drill guides might bend when axial forces are applied by surgeon during...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2023· T.A.G. MEDICAL PRODUCTS CORPORATION, LTD.

Recalled Item: BETTA LINK SR KNOTLESS IMPLANT KIT-Intended for use in soft Recalled by...

The Issue: Drill guides might bend when axial forces are applied by surgeon during...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2023· T.A.G. MEDICAL PRODUCTS CORPORATION, LTD.

Recalled Item: BETTA LINK SR REUSABLE FISHMOUTH GUIDE-Intended for use in soft Recalled by...

The Issue: Drill guides might bend when axial forces are applied by surgeon during...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2023· Olympus Corporation of the Americas

Recalled Item: Single Use Repositionable Clip QUICKCLIP PRO 165 CM 10/BX- Intended Recalled...

The Issue: Complaints on clip deployment occurring during clinical procedures, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2023· Olympus Corporation of the Americas

Recalled Item: Single Use Repositionable Clip QUICKCLIP PRO 165CM 5/BX- Intended for...

The Issue: Complaints on clip deployment occurring during clinical procedures, leading...

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

Class II — Potential Health HazardOngoing