EVIS EXERA III Duodenovideoscope
Brand(s)
Last updated
Summary
Product
EVIS EXERA III Duodenovideoscope
Issue
Medical devices - Labelling and packaging
What to do
Contact the manufacturer if you require additional information.
Audience
Healthcare
Affected products
Affected products |
Lot or serial number |
Model or catalogue number |
|---|---|---|
EVIS EXERA III Duodenovideoscope |
All lots. |
TJF-Q190V |
Issue
Olympus has updated the reprocessing materials to minimize potential deviations in TJF duodenoscope reprocessing. Olympus is informing users of these changes and is reminding users to closely follow the operation and reprocessing instructions. Users are required to acknowledge reviewing all such materials, which can be accessed through Olympus' education portal.
Additional information
Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Gastroenterology and urology
Companies
Olympus Medical Systems Corp.
2951 Ishikawa-Cho, Hachioji-Shi, Tokyo-To, Japan, 192-8507
Published by
Health Canada
Audience
Healthcare
Recall class
Type I
Recall date
Identification number
RA-81566
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