Product Wiki · Recalls · Health Canada — Medical Devices

MONACO — recall 56522

Health Canada — Medical Devices · Canada · 2017-01-25 · 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: 56522
Date of alert: 2017-01-25
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: Calculated dose from wedged beams can be assigned to the wrong beam. This can occur for a plan with at least two beams using the Elekta Motorized Wedge. The user must change the beam index numbers belonging to the two wedged beams, such that the index numbers have been exchanged for these beams, then edit the wedge angle of one of the beams. The beam index numbers are located in the first column of the beams spreadsheet.

Primary source: https://recalls-rappels.canada.ca/en/alert-recall/monaco-0

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.

MONACO — recall 56522

Related