Official recall record
EVIS EXERA Bronchovideoscopes
- Issuing authority
- Health Canada — Medical Devices
- Published
- 2023-11-20
- Country of alert
- Canada
- Alert level
- Type II
- Alert type
- recall
What the authority reported
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
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
Health Canada — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.
Record last checked against the registry on 2026-05-31.
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