Official recall record
LEO+ Intracranial Self Expandable Stent And Delivery System
- Issuing authority
- Health Canada
- Alert date
- 2026-09-02
- Country of alert
- Canada
- Alert level
- Type II
- Alert type
- recall
What the authority reported
As a precautionary measure, Balt Extrusion is voluntarily recalling specific ANRYV connector lots after routine quality control identified non-conforming bacterial endotoxin test results. The recall affects both standalone ANRYV connectors and ANRYV connectors incorporated into selected Balt product kits, despite no reported patient harm to date.
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 2026-09-12.
Record last checked against the registry on 2026-09-12.
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