Product Wiki · Recalls · Health Canada — Medical Devices

Onpoint Scope Procedure Kit & Arthrosimplicity Kit (2020-09-11) — recall 61635

Health Canada — Medical Devices · Canada · 2020-09-25 · Type II

Compiled from an official source — the facts on this page are reproduced from the issuing authority’s own published notice, which is linked above. No AI-generated text appears on this page. How we use AI →
Agency
Health Canada — Medical Devices
Recall identifier
61635
Date of alert
2020-09-25
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Reported risk: Zimmer Biomet is conducting a lot specific medical device recall for the Regenerex Taper Cap, the Onpoint Scope Procedure Kit and the Arthrosimplicity Kit due to the items not properly being aligned with the adequate gamma sterilization group. This could result in the product not being properly sterilized. The syringe pump tubing sets in the kits are affected, but the entire kits listed in the affected must be returned. This issue was identified during the annual family review for sterile product.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/onpoint-scope-procedure-kit-ar

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.

Related

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.