Brand

Medtronic, Inc.: official recall notices

6 official recall or safety notices on this site name Medtronic, Inc., dated between 2025-04-29 and 2026-03-11. They were issued by 1 authority: US FDA — Medical Devices (6).

Countries where the notices were issued: United States (6).

Name as written in the notices: Medtronic, Inc.. This is the brand or the responsible company as each authority recorded it. A recall shows a safety system working; it is not a verdict on a brand. Follow the official notice for each product.

Notices by year

Year	Notices
2026	1
2025	5

Notices by authority

Authority	Notices
US FDA — Medical Devices	6

All notices

Date	Authority	Product	Hazard (as classified)
2026-03-11	US FDA — Medical Devices	Medtronic Sphere-9 Catheter, Model Number AFR-00001; catheter, percutaneous, cardiac ablation, for treatment of atrial f	—
2025-06-18	US FDA — Medical Devices	Medtronic CareLink SmartSync Patient Connector, Model Number 24967 with the following software components: 1. Cobalt	—
2025-06-18	US FDA — Medical Devices	Medtronic CareLink SmartSync Device Manager, Model Number 24967A with the following software components: 1. Cobalt Cr	—
2025-06-17	US FDA — Medical Devices	Medtronic SmartLink Software loaded on SmartSync Patient Connector, Model Number 24967 with the following software compo	—
2025-06-17	US FDA — Medical Devices	Medtronic SmartLink software loaded on CareLink SmartSync Device Manager, Model Number 24967A with the following softwar	—
2025-04-29	US FDA — Medical Devices	Azure S DR MRI SureScan, Product number W3DR01	—

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