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[Recalled] Olympus Bronchovideoscope, Models BF-3C40 & BF-N20. — Complaint of endoscope model becoming lodged in the endotracheal tube connector… | FDA 2023-07-27

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 Bronchovideoscope, Models BF-3C40 & BF-N20.
Brand / manufacturerOlympus Corporation of the Americas
Categorydevice
Issuing authorityFDA_DEVICE
ReferenceZ-2502-2023
Country of noticeUnited States
Risk levelClass II
Hazard typerecall
Notice date27 July 2023
EAN / barcode04953170308130

Why it was recalled

According to the FDA_DEVICE notice, the identified hazard is: Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.

This Class II 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

Check whether your unit is affected and follow the authority's guidance before further use.

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.

Shop Recalled Olympus Bronchovideoscope Models
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