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 80618080 of 28,538 recalls

Medical DeviceMay 25, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: MERIT MEDICAL SYSTEMS Temno Soft Tissue Biopsy Device Temno 14 Recalled by...

The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: COOPER SURGICAL Milex PESSARY Recalled by Mckesson Medical-Surgical Inc....

The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: Mckesson GYNECATH H/S CATHETER 5FR (10/CS) Model Number: 11-19610 Recalled...

The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: MEDLINE INDUSTRIES Medline Catheter Insertion Tray Medline Foley Without...

The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: Fischer Cone Biopsy Excisor EXCISOR Recalled by Mckesson Medical-Surgical...

The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: 3M COMPANY 3M PAD Recalled by Mckesson Medical-Surgical Inc. Corporate...

The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: MORRISON MEDICAL Morrison Medical OB KIT Recalled by Mckesson...

The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: Dynarex SWAB Recalled by Mckesson Medical-Surgical Inc. Corporate Office Due...

The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: a. Alcon Clear Care Contact Lens Solution Clear Care 12 oz. Solution...

The Issue: Facility Temperature excursions (from June 2021-August 2021) prior to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2022· Cook Incorporated

Recalled Item: Pressure Monitoring Set Recalled by Cook Incorporated Due to The products...

The Issue: The products may contain excess coating material on the outside and/or...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2022· Tandem Diabetes Care Inc

Recalled Item: t:slim X2 insulin pump Recalled by Tandem Diabetes Care Inc Due to Insulin...

The Issue: Insulin pumps may have the following issues: 1) Malfunction 6 Non-Volatile...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2022· CareFusion 303, Inc.

Recalled Item: BD Pyxis MedBank Cabinet Software v2.1.2.9 Legacy MedBank Cabinets with...

The Issue: The automated dispensing cabinet software update included a .dll file that...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2022· Tandem Diabetes Care Inc

Recalled Item: t:slim X2 insulin pump Recalled by Tandem Diabetes Care Inc Due to Insulin...

The Issue: Insulin pumps may have the following issues: 1) Malfunction 6 Non-Volatile...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2022· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: Tibial Component Modular. orthopedic prosthesis. Model Nos: Small Recalled...

The Issue: There is a risk that blind screws of the modular tibial component cannot be...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2022· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: Endo Model Modular Rotational Tibia - Small (Model No #15-2814/02) Recalled...

The Issue: There is a risk that blind screws of the modular tibial component cannot be...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2022· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: Endo Model Modular Femur and Tibia Recalled by Waldemar Link GmbH & Co. KG...

The Issue: There is a risk that blind screws of the modular tibial component cannot be...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2022· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: Tibial Component. orthopedic prosthesis. Model Nos: Small Recalled by...

The Issue: There is a risk that blind screws of the modular tibial component cannot be...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zeego (Model no. 10280959) and Artis Q.zeego (Model no. 10848283)...

The Issue: It may occur that after system startup no stand movement is possible any...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2022· Dental Choice Holding Llc

Recalled Item: CustMbite Recalled by Dental Choice Holding Llc Due to The device was...

The Issue: The device was marketed and sold in the US without FDA clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2022· Medtronic MiniMed

Recalled Item: MiniMed 640G Insulin Pump (O.U.S. Version) Recalled by Medtronic MiniMed Due...

The Issue: Due to battery cap deterioration, this may potentially result in an...

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

Class II — Potential Health HazardOngoing