CareLink SmartSync Programmer Recall: Software Issue
CareLink SmartSync Programmer, Model 24970A, Pulse generator, permanent, implantable
What is the FDA recall status?
The FDA record lists this recall as ongoing. FDA enforcement data is not a live recall-lifecycle tracker. Follow the official instructions and check the agency notice or firm for current guidance.
Why was CareLink SmartSync Programmer recalled?
Software problem has the potential for an inaccurate displayed longevity estimate.
What should I do if I have this product?
Follow the firm and FDA instructions for the affected product. Contact the recalling firm for current guidance.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
The official FDA identifier list is too long to reproduce here. Compare your item with the complete list in the agency notice.
Full product description
CareLink SmartSync Programmer, Model 24970A, Pulse generator, permanent, implantable
Which lot codes, UPCs or models are affected?
The official FDA record has an unusually long identifier list. Check the complete lot, serial and model numbers in the linked agency notice.
Open the complete official FDA record
- Agency record number
- Z-0302-2027
- Product
- CareLink SmartSync Programmer, Model 24970A, Pulse generator, permanent, implantable
- Recalling firm
- Medtronic, Inc.
- Quantity
- 11238 units
- Distribution
- Worldwide distribution.
- Recall started
- September 24, 2026
- Report date
- November 4, 2026
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)