Product Wiki · Recalls · Health Canada — Medical Devices

Philips Achieva, Intera and Ingenia Systems — recall 74922

Health Canada — Medical Devices · Canada · 2024-01-17 · Type I

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
74922
Date of alert
2024-01-17
Country / jurisdiction
Canada
Risk level
Type I
Risk type
recall
Product category
Radiology
Product type
Medical devices
Reported risk: The quadrature body coil (QBC) seal adhesive may fail creating sharp edges that may come in contact with patients. The QBC seal may become loose as the patient table travels in a horizontal motion in and out of the system bore. The QBC seal (figure 1) is a rubber seal that is glued between the cone cover and QBC cover and functions to prevent sharp edges of the QBC cover from contacting patients during an examination. Recall start date: January 9, 2024
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/philips-achieva-intera-and-ing

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.