Product Wiki · Recalls · Health Canada — Medical Devices

Iris X80, X90, and PXL Intra-Oral Cameras — recall 76776

Health Canada — Medical Devices · Canada · 2024-12-30 · 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
76776
Date of alert
2024-12-30
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
General and plastic surgery - General hospital and personal use
Product type
Medical devices
Reported risk: Class II medical device sold and distributed as a class I medical device. No defects or known safety related issues. Recall Start Date: December 12, 2024
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/iris-x80-x90-and-pxl-intra-ora

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.