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[Recalled] Olympus BRONCHOFIBERSCOPE BF Type, Model Numbers BF-PE2, BF-TE2 — There have been complaints of endobronchial combustion during therapeutic laser… | FDA 2023-06-08

recall fda device united-states

The product on this page is subject to an official recall. We summarise the regulator's findings and the recommended action.

Recall details

ProductOlympus BRONCHOFIBERSCOPE BF Type, Model Numbers BF-PE2, BF-TE2
Brand / manufacturerOlympus Corporation of the Americas
Categorydevice
Issuing authorityFDA_DEVICE
ReferenceZ-2012-2023
Country of noticeUnited States
Risk levelClass I
Hazard typerecall
Notice date08 June 2023
EAN / barcode04953170339974

Why it was recalled

According to the FDA_DEVICE notice, the identified hazard is: There have been complaints of endobronchial combustion during therapeutic laser procedures with the bronchoscope.

This Class I recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.

What to do if you own this product

Stop using the product immediately and follow the authority's remedy (return, repair, or disposal).

Read the full official notice →

Related recalls from Olympus Corporation of the Americas

This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.

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