Health product recall

Evis Exera Video System and OES - Bronchoscopes

Last updated

Summary

Product
Evis Exera Video System and OES - Bronchoscopes
Issue
Medical devices - Device compatibility
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-Q180
BF-1T180

Evis Exera Video Sytem - Bronchovideoscope

All lots.

BF-XT160

OES Bronchofiberscopes

All lots.

BF-P60
BF-1T60
BF-MP60

Evis Exera III Video System - Bronchovideoscope

All lots.

BF-Q190
BF-1TH190
BF-H190
BFXT190

Issue

Olympus has received complaints of endobronchial combustion during therapeutic procedures using lasers or argon plasma coagulation with the Olympus bronchoscope. If endobronchial combustion occurs, patients may suffer internal burn in their airway or lungs, respiratory insufficiency, apnea, loss of consciousness, hospitalization or its prolongation, ICU care, or death.

Three (3) adverse event complaints with endobronchial combustion during laser or argon plasma coagulation procedures have occurred, of which one (1) complaint resulted in patient death. In an effort to maximize patient safety and mitigate any potential risk to patient health, Olympus is notifying users of these complaints and the providing the following recommendations related in combination with laser therapy equipment:

- Only Nd:YAG laser or 810 nm diode lasers may be used with Olympus laser compatible bronchoscopes. Olympus has not evaluated any other lasers for compatibility with the indicated bronchoscope models

- Do not perform laser cauterization while supplying oxygen. This may result in combustion during cauterization. This is included in the warnings in the operation manual on laser cauterization with Olympus bronchoscopes.

- Never emit laser radiation before confirming that an appropriate distance between the target and the endoscope's distal end with the tip of the laser probe is in the correct position in the endoscopic image. This is essential to avoid patient injury (burns, bleeding, & perforation) or damage to the device.

Recall start date: June 30, 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 & 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
Identification number
RA-73939

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