Product Wiki · Recalls · Health Canada — Medical Devices

Phoroptor VRx Digital Refraction System — recall 74241

Health Canada — Medical Devices · Canada · 2023-09-08 · 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
74241
Date of alert
2023-09-08
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Ophthalmology
Product type
Medical devices
Reported risk: Some Phoroptor VRx devices may have an assembly defect that causes the device to detach from the bracket that connects it to an ophthalmic stand. A device that detaches from a stand can fall on to a patient or operator causing an injury. The defect was identified via a customer complaint received on April 3, 2023. The subsequent complaint investigation showed that other units built in December 2021 and January 2022 could have the same defect. Recall Start Date: August 11, 2023
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/phoroptor-vrx-digital-refracti

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.