Product Wiki · Recalls · Health Canada — Medical Devices

EDS Light Suspension, Central Axis For Visum Led Surgical Light — recall 56576

Health Canada — Medical Devices · Canada · 2017-03-24 · 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
56576
Date of alert
2017-03-24
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Notice status
Archived by the issuing authority — kept for reference
Reported risk: Stryker has become aware that there is a remote likelihood that the EDS Light Suspension, Central Axis may have an insufficiently assembled joint in the suspension. The EDS Systems have redundant connections throughout the suspensions. If the EDS Light Suspension, Central Axis falls, it could potentially cause serious injuries to healthcare providers and/or patients. To date, there have been no adverse events reported for this issue.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/eds-light-suspension-central-a

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.