Official recall record
InterStim™ Systems
- Issuing authority
- Health Canada
- Alert date
- 2026-09-24
- Country of alert
- Canada
- Alert level
- Type II
- Alert type
- recall
What the authority reported
Medtronic has received 15 complaints involving the selection of an incompatible component based on the intended system configuration between 01-Jan-2020 through 12-Aug-2026. Use of an incompatible lead or percutaneous extension has resulted in a delay of surgery or the need for surgical replacement of the component. Review of complaint data confirmed that the product is functioning as designed and there are no device or product performance issues.
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.
Verify at the source:
Health Canada — official record →
Record last checked against the registry on 2026-09-29.
Record last checked against the registry on 2026-09-29.
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