Official recall record

Medtronic CareLink SmartSync Patient Connector, Model Number 24967 with the following software components: 1. Cobalt Crome application, S

What the authority reported

In prior SmartSync application versions, the Abort button stopped the test that was selected. During an induction test, there was a limited window of time for the user to abort a therapy, thereby limiting the user's ability to cancel a high voltage therapy delivery.

What to do

Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.

More recalls: US FDA — Medical Devices · United States · all filters

Same barcode in other registries

The same EAN appears in 3 other official recall record(s) — a cross-border signal worth checking if you bought this product abroad.

• 2025-06-17 · US FDA — Medical Devices
  Medtronic SmartLink Software loaded on SmartSync Patient Connector, Model Number 24967 with the following software compo
• 2025-06-18 · 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 CareLink SmartSync Device Manager, Model Number 24967A with the following softwar

Other recalls from this brand

• 2026-03-11 · US FDA — Medical Devices
  Medtronic Sphere-9 Catheter, Model Number AFR-00001; catheter, percutaneous, cardiac ablation, for treatment o
• 2025-06-18 · US FDA — Medical Devices
  Medtronic CareLink SmartSync Device Manager, Model Number 24967A with the following software components: 1.
• 2025-06-17 · US FDA — Medical Devices
  Medtronic SmartLink Software loaded on SmartSync Patient Connector, Model Number 24967 with the following soft

All 6 official recall notices naming Medtronic, Inc. on this site →