OFFICIAL-SOURCE RECALL · CANADA
LEO+ Intracranial Self Expandable Stent And Delivery System Recall: As a precautionary measure, Balt
Use the identifiers printed on your item to determine whether this recall may affect the product you own.
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Is your product affected?
- Brand
- See official notice
- Product
- LEO+ Intracranial Self Expandable Stent And Delivery System
- Manufacturer
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The barcode may identify the product type, while the recall may apply only to certain lots, dates or variants. Check all identifiers listed in the official recall.
Why this product was recalled
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.
Hazard
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.
Official recall notice
LEO+ Intracranial Self Expandable Stent And Delivery System
Agency: Health Canada
Official publication date: September 2, 2026
Read the official CANADA_MEDICAL_DEVICES recall notice →SCAN ONCE. KEEP WATCHING.
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