Medtronic, Inc.: Pulse Generator, Permanent, Implantable
Recall Summary Medtronic is recalling the CareLink SmartSync Programmer, Model 24970A, a device used with implantable pulse generators, because a software problem can display inaccurate battery life estimates. This recall affects pulse generator devices that have been distributed worldwide. The recall is classified as Class III, indicating a potential health hazard.
- Recalling firm
- Medtronic, Inc.
- Product
- CareLink SmartSync Programmer, Model 24970A, Pulse generator, permanent, implantable
- Reason
- Software problem has the potential for an inaccurate displayed longevity estimate.
- Classification
- Class III
- Category
- medical device recall
- Country
- United States
- Agency
- FDA-DEVICES
- Recall date
- 2026-09-24
- Status
- Open, Classified
- Distribution
- Worldwide distribution.
Official recall notice from FDA-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/a3d6cf1b-629f-4363-9ffc-858ff1da4176