Product Wiki · Recalls · Health Canada — Medical Devices

Zenith Alpha Spiral-Z Endovascular Leg (2020-01-14) — recall 63111

Health Canada — Medical Devices · Canada · 2020-01-31 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
63111
Date of alert
2020-01-31
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Reported risk: This is a product notification and is for information purposes only. No devices need to be returned. Customers are being advised to follow key points in the IFU to avoid thrombus formation and/or lumen occlusion while using the Zenith Alpha¿ Spiral-Z® Endovascular Leg on patients. A copy of an updated Planning and Sizing Worksheet is also being provided to customers.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/zenith-alpha-spiral-z-endovasc

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.