Medtronic, Inc. 2025-07-30 Health serious FDA
Health · FDA · Recall #FDA-Z-2168-2025
Medtronic CareLink SmartSync Patient Connector, Model Number 24967 with the following… Recall
Issued July 30, 2025 · Medtronic, Inc.
In July 2025, Medtronic, Inc. recalled the Medtronic CareLink SmartSync Patient Connector, Model Number 24967 with the following…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
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 you should do
- 1 Stop using Medtronic CareLink SmartSync Patient Connector, Model Number 24967 with the following… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Medtronic, Inc. to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Medtronic, Inc.
- Category
- Health
- Recall date
- July 30, 2025
- Units affected
- Not reported
- Sold at
- Worldwide - US Nationwide distribution.
- Recall number
- FDA-Z-2168-2025
- Made in
- United States
- Issuing agency
- FDA
In context
- Medtronic, Inc. has 3 recalls in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 691st Health recall we've logged in 2025.