Product Wiki · Recalls · Health Canada — Medical Devices

Rusch Greenlite (2020-01-15) — recall 63114

Health Canada — Medical Devices · Canada · 2020-01-31 · 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
63114
Date of alert
2020-01-31
Country / jurisdiction
Canada
Authority classification
Type II
Notice type
recall
Product category
Medical devices
Product type
Medical devices
Reported risk: Teleflex has received complaints that the lights guide of the Rusch Greenlite Mac Laryngoscope broke at the point of a welded joint either prior to use during setup or during use inside the patients mouth.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/rusch-greenlite-2020-01-15

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.