Product Wiki · Recalls · Health Canada — Medical Devices

Optima X-Ray Systems (2013-12-05) — recall 50748

Health Canada — Medical Devices · Canada · 2014-03-18 · 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 on this page. No AI-generated text appears on this page. How we use AI →
Agency
Health Canada — Medical Devices
Recall identifier
50748
Date of alert
2014-03-18
Country / jurisdiction
Canada
Authority classification
Type III
Notice type
recall
Product category
Medical devices
Product type
Medical devices
Notice status
Archived by the issuing authority — kept for reference
Reported risk: Intermittently when a large number of patient exams are retrieved from the HIS/RIS system, the exams when displayed on the mobile X-ray system are not properly displayed. If the user continues to attempt to select one of the exams when this issue has occurred, the system will update the screen and in doing so, potentially select a different exam/patient.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/optima-x-ray-systems-2013-12-0

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.

Related

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.