Product Wiki · Recalls · Health Canada — Medical Devices

PINPOINT Endoscopic Fluorescence Imaging System (Operator Manual)… — recall 54908

Health Canada — Medical Devices · Canada · 2016-05-25 · Type I

As described by Health Canada — Medical Devices: PINPOINT Endoscopic Fluorescence Imaging System (Operator Manual) (2016-01-29)

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
54908
Date of alert
2016-05-25
Country / jurisdiction
Canada
Risk level
Type I
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Notice status
Archived by the issuing authority — kept for reference
Reported risk: Operator manual is being recalled since it does not contain validated parameters for gravity-cycle autoclave sterilization of the PINPOINT laparoscopes and light guide cable in the reprocessing tray.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/pinpoint-endoscopic-fluorescen

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.