Product Recalls in Minnesota

Product recalls affecting Minnesota — including food, drugs, consumer products, medical devices, and vehicles distributed to Minnesota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,654 recalls have been distributed to Minnesota in the last 12 months.

52,120 total recalls
2,654 in last 12 months

Showing 81618180 of 29,186 recalls

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

Recalled Item: a. ABBOTT RAPID DX N AMERICA LLC Alere Rapid Test 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¿ PAD 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: 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