Product Wiki · Recalls · Health Canada — Medical Devices

ELLEX INTEGRA PRO LP5532 (2016-03-16) — recall 54735

Health Canada — Medical Devices · Canada · 2016-04-04 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
54735
Date of alert
2016-04-04
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: Under certain conditions there is a potential for the glass of the safety filter optics to crack on their lower edge due to pressure applied on them by their retaining plate which in turn could damage the laser safety coating on the optics. If this occurs, there is a remote possibility the user could be exposed to any diffused reflected laser light during laser treatment.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/ellex-integra-pro-lp5532-2016-

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