[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
The product on this page is subject to an official recall. We summarise the regulator's findings and the recommended action.
Recall details
| Product | Olympus BRONCHOFIBERSCOPE BF Type, Model Numbers BF-PE2, BF-TE2 |
|---|---|
| Brand / manufacturer | Olympus Corporation of the Americas |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-2012-2023 |
| Country of notice | United States |
| Risk level | Class I |
| Hazard type | recall |
| Notice date | 08 June 2023 |
| EAN / barcode | 04953170339974 |
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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