Reported Sep 6, 2023 · Ongoing
Olympus Bronchovideoscope, Models BF-MP160F, BF-XP160F, BF-XP60.
Olympus Corporation of the Americas
Moderate riskThis product could cause temporary or reversible health problems — stop using it.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 BronchovideoscopeModels BF-MP160FBF-XP160FBF-XP60
- Lot codes and dates
- UDI-DI
049531703400480495317028906404953170340093049531702890330495317034011604953170308154& 04953170339240All Serial Numbers
- UDI-DI
- Amount recalled
- 1072 units
This recall covers 17 products
The agency filed one notice per product. You are reading one of them; the other 16 are below.
4 more are in the archive.
Where it was sold
- Nationwide
Why it was recalled
Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.
This product could cause temporary or reversible health problems — stop using it.
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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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