Health Canada — Medical Devices · Canada · 2016-08-26 · 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 →
Archived by the issuing authority — kept for reference
Reported risk: When using the perpendicular line tool there is an option to "snap" the lines together which prevents the perpendicular lines from extending past the straight/base line. While the system default is set to snap the lines together, the actual "snap" function may not occur until the plan is saved, at which time the line end point within 20 pixels of the base line will adjust its location to snap perfectly to the base line. This may adjust the length and corresponding measurement of the perpendicular line when the plan is reopened.
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.