Product Wiki · Recalls · Health Canada — Medical Devices

LeoniPlus and LeoniPlus with HFO (2014-11-05) — recall 52858

Health Canada — Medical Devices · Canada · 2014-11-21 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
52858
Date of alert
2014-11-21
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: If contrary to the instruction for use, the display is cleaned with liquids instead of wiping with an approved cleaning agent, ingress of such liquids may lead to malfunction of the keypad identified as a permanent or a mission function of the keys. Do not use machine.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/leoniplus-and-leoniplus-hfo-20

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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.