Product Wiki · Recalls · Health Canada — Medical Devices

Chromophare Surgical Lighting System — recall 81701

Health Canada — Medical Devices · Canada · 2026-03-05 · 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
81701
Date of alert
2026-03-05
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
General and plastic surgery
Product type
Medical devices
Reported risk: Stryker has discovered that certain lots of the soffit ring may not adequately support the weight of the ceiling cover. As a result, the cover may shift or slide down the ceiling tube. Movement of the ceiling cover can expose the area above the ceiling, which may allow particles, such as dust, debris, residue, or other contaminants, to enter the sterile field.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/chromophare-surgical-lighting-

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.

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.