Medtronic, Inc. recalls

9 recalls on record · latest: March 11, 2026

Official U.S. recall history for Medtronic, Inc., compiled from official government records.

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Medtronic, Inc. recalls Medtronic Sphere-9 Catheter, Model Number AFR-00001; catheter, percutaneous, cardiac ablation, for treatment of atrial…

March 11, 2026 · Medical device recalls Moderate risk ventricular fibrillation (VF) during radiofrequency (RF) therapy with the Medtr…

Medtronic Inc recalls Abre Venous Self-Expanding Stent System, Model numbers AB9G14120090 AB9G12100090 AB9G14080090 AB9G12080090 AB9U12060090…

December 4, 2025 · Medical device recalls Moderate risk Stents may be impacted by a Nitinol anomaly which causes a reduced stent diamet…

Medtronic, Inc. recalls Aurora EV-ICD and Clinical EV-ICD, single chamber, extravascular implantable cardioverter defibrillators (ICD), Product…

October 29, 2025 · Medical device recalls Moderate risk There is a potential for delayed time to high-voltage (HV) therapy should a rar…

Medtronic, Inc. recalls Medtronic CareLink SmartSync Device Manager, Model Number 24967A with the following software components: 1. Cobalt Crom…

June 18, 2025 · Medical device recalls Moderate risk In prior SmartSync application versions, the Abort button stopped the test that…

Medtronic, Inc. recalls Medtronic CareLink SmartSync Patient Connector, Model Number 24967 with the following software components: 1. Cobalt Cr…

June 18, 2025 · Medical device recalls Moderate risk In prior SmartSync application versions, the Abort button stopped the test that…

Medtronic, Inc. recalls Medtronic SmartLink software loaded on CareLink SmartSync Device Manager, Model Number 24967A with the following softwa…

June 17, 2025 · Medical device recalls Moderate risk A software update for Medtronic CareLink SmartSync Device Manager (SmartSync) i…

Medtronic, Inc. recalls Medtronic SmartLink Software loaded on SmartSync Patient Connector, Model Number 24967 with the following software comp…

June 17, 2025 · Medical device recalls Moderate risk A software update for Medtronic CareLink SmartSync Device Manager (SmartSync) i…

Medtronic, Inc. recalls Azure S DR MRI SureScan, Product number W3DR01

April 29, 2025 · Medical device recalls Moderate risk Identified devices may experience sudden battery power failure without alarm, p…

Medtronic Inc. recalls 2090 Programmers with serial number prefixes PKK0 and PKK1: a) 2090, Product Description: PRGM 2090 PROGRAMMER-PORTABLE…

July 11, 2024 · Medical device recalls Moderate risk Medtronic CareLink 2090 programmers with serial number prefixes PKK0 and PKK1 h…