Product Wiki · Recalls · Health Canada — Medical Devices

Blueprint Mixed Reality BP MxR Glenoid Pin Guide — recall 76680

Health Canada — Medical Devices · Canada · 2024-12-11 · 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
76680
Date of alert
2024-12-11
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Neurology
Product type
Medical devices
Reported risk: During product complaint review (July 2024), Stryker has identified an issue that impacts specific lots of Blueprint® Mixed Reality Glenoid Pin Guides. For the impacted pins guides, the metallic tube may disassemble from the plastic handle. This can result in the Blueprint Mixed Reality headset from being able to detect the Blueprint Mixed Reality Glenoid Pin Guide. Recall Start Date: November 26, 2024
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/blueprint-mixed-reality-bp-mxr

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.