GlideScope Video Laryngoscopes (2020-01-27) — recall 63182
Health Canada — Medical Devices · Canada · 2020-02-28 · Type III
🏛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 →
Reported risk: The outer shipping carton label was missing the international symbols that are printed adjacent to the accompanying text. The immediate device labels on all products are correct including all applicable symbols. There is no patient or user safety risk associated with the missing symbols. The missing symbols were discovered during a quality assurance finished product inspection at Verathon, Inc. headquarters in Bothell, WA. USA.
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.