Product Wiki · Recalls · Health Canada — Medical Devices

ALLURA XPER FD (2015-06-22) — recall 53986

Health Canada — Medical Devices · Canada · 2015-07-17 · 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
53986
Date of alert
2015-07-17
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Notice status
Archived by the issuing authority — kept for reference
Reported risk: Philips had received a call with respect to an issue with a failing Monitor Ceiling Suspension (MCS) actuator of an Allura Xper system. The actuator assembly had become detached and the monitor carriage with a FlexVision monitor dropped to its lowest position. The monitor ceiling suspension is designed to allow flexible positioning near the patient table when in use, and away from the patient when not in use. (Park position).
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/allura-xper-fd-2015-06-22

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.