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Evis exera video system and oes - bronchoscopes

Official notice

12 Jul 2023

Last checked

12 Jul 2023

Critical riskHealth Canada

An official Health Canada notice concerns Evis exera video system and oes - bronchoscopes. 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 Published 2023-07-12.

What to do now

Contact the manufacturer if you require additional information.

Recall number

73939

Official notice

2023-07-12

The hazard

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

How to check if you're affected

Compare the product name and identifiers below with the item you own. Follow the official notice if they match.

Recall Numbers

73939

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Affected products

Product 1

Affected products - Evis Exera II Video System - Bronchovideoscopes, Lot or serial number - All lots., Model or catalog number - BF-1TQ180 BF-P180 BF-Q180-AC BF-Q180 BF-1T180

Product 2

Affected products - Evis Exera Video Sytem - Bronchovideoscope, Lot or serial number - All lots., Model or catalog number - BF-XT160

Product 3

Affected products - OES Bronchofiberscopes, Lot or serial number - All lots., Model or catalog number - BF-P60 BF-1T60 BF-MP60

Product 4

Affected products - Evis Exera III Video System - Bronchovideoscope, Lot or serial number - All lots., Model or catalog number - BF-Q190 BF-1TH190 BF-H190 BFXT190

Risk / hazard

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

Where it was sold

The source does not list specific retailers. See the official notice for where affected products were sold.

Location 1

CA · Canada

Affected area 1

CA · Canada

Company & contacts

Manufacturer

Not provided

Phone

Not provided

Brand: Olympus Medical, Evis Exera Video System And Oes - Bronchoscopes.

Source & status

Source

Health Canada

Tier

official

Category

HOME

Classification

Type I

App estimate

critical

Recall details

Recall number

73939

Classification

Type I

Source tier

official

Documents, notices & source

See the official notice and source documents for full details.

View full official notice
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