Product Wiki · Recalls · Health Canada — Medical Devices

OER-PRO ENDOSCOPE REPROCESSOR (2016-06-16) — recall 55193

Health Canada — Medical Devices · Canada · 2016-07-19 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
55193
Date of alert
2016-07-19
Country / jurisdiction
Canada
Authority classification
Type II
Notice type
recall
Product category
Medical devices
Product type
Medical devices
Notice status
Archived by the issuing authority — kept for reference
Reported risk: OER-Pro operation manual has been revised to add a new warning requiring users to conduct precleaning and manual cleaning as detailed in the duodenoscope's reprocessing manual(s).
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/oer-pro-endoscope-reprocessor-

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