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Official recall record

Axonics SNM System® - Tined Lead

Health Canada — Medical Devices · 2025-10-22 · CanadaType II
Issuing authority
Health Canada — Medical Devices
Published
2025-10-22
Country of alert
Canada
Alert level
Type II
Alert type
recall

What the authority reported

Boston Scientific is writing to share information related to the tined lead component of the Axonics SNM System® Tined Lead Kit (model 1201). Boston Scientific has identified that in a small percentage of cases, users may experience difficulty advancing the tined lead through the introducer sheath during implantation, requiring device exchange during the procedure. Investigation determined that difficulty advancing the lead may be due to the amount of adhesive applied to the tine component during manufacturing, which may prevent them from fully deflecting within the sheath. Boston Scientific has since introduced controls to prevent this issue occurring in the future. This issue only affects sheath compatibility; the performance of implanted tined lead devices is not affected.

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 — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.

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