Reported Jul 26, 2023 · Ongoing
Olympus BRONCHOFIBERSCOPE BF Type, Model Numbers BF-PE2, BF-TE2
Olympus Corporation of the Americas
High riskUsing this product could cause serious injury, illness or death — stop using it now.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Olympus Corporation of the Americas · 3500 Corporate Pkwy · Center Valley, PA · 18034-8229
Is this the product you have?
Olympus BRONCHOFIBERSCOPE BF TypeModel Numbers BF-PE2BF-TE2
- Lot codes and dates
- All serial numbers BF-PE2 BRONCHOFIBERSCOPE
- OLYMPUS BF TYPE PE2 UDI04953170339974 BF-TE2 BRONCHOFIBERSCOPE
- OLYMPUS BF TYPE TE2 UDI04953170339998
- Amount recalled
- 4 units
This recall covers 7 products
The agency filed one notice per product. You are reading one of them; the other 6 are below.
Where it was sold
- Nationwide
Why it was recalled
Stop using this product now
There have been complaints of endobronchial combustion during therapeutic laser procedures with the bronchoscope.
Using this product could cause serious injury, illness or death — stop using it now.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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