⚠ RecallRadar📷 ScanGuidesOfficial U.S. recall notices, restated plainly

Medtronic recalls - full list & free alerts

3 official U.S. recalls involving Medtronic in the last 12 months, most recently on 2026-05-06.

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Full list (3)

Medtronic, Inc.: Medtronic Sphere-9 Catheter, Model Number AFR-00001; catheter, percutaneous, cardiac ablation, for treatment of atrial flutter.
Medical DevicesFDA (device) · 2026-05-06 · Class II
Medtronic Inc: Abre Venous Self-Expanding Stent System, Model numbers AB9G14120090 AB9G12100090 AB9G14080090 AB9G12080090 AB9U12060090 AB9U14100090 A
Medical DevicesFDA (device) · 2026-01-21 · Class II
Medtronic, Inc.: Aurora EV-ICD and Clinical EV-ICD, single chamber, extravascular implantable cardioverter defibrillators (ICD), Product Number DVEA3E4
Medical DevicesFDA (device) · 2025-12-10 · Class II