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

Is Medtronic recalled?

Medtronic recalls - full list & free alerts

Official U.S. agency records list 3 recalls involving Medtronic in the last 12 months, most recently on 2026-05-06. Check each official notice for the exact products, lot codes and dates affected.

Check a lot code, UPC or model number

This is not a guarantee; check the official notice.

Recalls (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
Free daily digest + "My products" watchlist

Get the daily digest, and tell us what to watch. Everything is optional except your email.

Free allergen alerts:

Categories:

Privacy: we store only what you enter here, use it only to send recall alerts you asked for, never sell or share it, and you can unsubscribe anytime. Double opt-in: we will email you a confirmation link before sending anything; alerts start only after you confirm. Every email has unsubscribe and manage-watchlist links.