FABIUS Tiro Anesthesia System, GS Premium System and MRI (2017-11-01) — recall 57792
Health Canada — Medical Devices · Canada · 2017-11-15 · Type I
🏛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 →
Archived by the issuing authority — kept for reference
Reported risk: Draeger has become aware of information suggesting that the use of the Auxiliary Common Gas Outlet (ACGO) at anesthesia workstations of different manufacturers was not performed as described in the instructions for use of the relevant manufacturer, and not according to published safety guidelines (pre-use checklist) from various anesthesia societies.
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.