EVIS EXERA Bronchovideoscopes
Brand(s)
Last updated
Summary
Product
EVIS EXERA Bronchovideoscopes
Issue
Medical devices - Performance
What to do
Contact the manufacturer if you require additional information.
Audience
Healthcare
Affected products
| Affected products | Lot or serial number | Model or catalog number |
|---|---|---|
| EVIS EXERA II Video System - Bronchovideoscopes | All lots. | BF-1TQ180 BF-P180 BF-Q180-AC BF-1T180 |
| EVIS EXERA III Video System - Bronchovideoscopes | All lots. | BF-XT190 BF-P190 BF-1TH190 BF-H190 BF-Q190 |
Issue
Olympus has received four (4) adverse event complaints of endobronchial combustion during therapeutic procedures with the Olympus bronchoscope model BF-XT190, of which one (1) involved high-frequency therapy equipment. the other three (3) adverse events involved unknown energy therapy equipment. There are a total of 28 models of the BF series endoscopes that can be used in combination with high-frequency therapy equipment
Recall start date: October 27, 2023
Additional information
Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Ear, nose and throat
Health products - Medical devices - Gastroenterology and urology
Health products - Medical devices - General and plastic surgery
Companies
Olympus Medical Systems Corp.
2951 Ishikawa-Cho, Hachioji-Shi, Tokyo-To, Japan, 192-8507
Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-74619
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