Product Wiki · Recalls · Health Canada — Medical Devices

SERIES 200 ELECTRONIC VIDEO ENDOSCOPE SYSTEM (2015-06-30) — recall 53764

Health Canada — Medical Devices · Canada · 2015-09-08 · Type III

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Agency
Health Canada — Medical Devices
Recall identifier
53764
Date of alert
2015-09-08
Country / jurisdiction
Canada
Risk level
Type III
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Notice status
Archived by the issuing authority — kept for reference
Reported risk: Fujifilm has become aware that the EPX-2500 operation manual and sales brochure incorrectly identify that the ED-530XT endoscope is capable of being used with the EPX- 2500 processor. The operation manual and sales brochure state that when the ED- 530XT endoscope is used with the 2500 processor, a "super image" is displayed, when it is actually a "standard image" that is displayed.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/series-200-electronic-video-en

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