Reported Sep 6, 2023 · Ongoing
EVIS EXERA III DUODENOVIDEOSCOPE OLYMPUS TJF-Q190V
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?
- EVIS EXERA III DUODENOVIDEOSCOPE OLYMPUS TJF-Q190V
- Lot codes and dates
- Model No. TJF-Q190V
- UDI-DI04953170405563; All Serial No
- Amount recalled
- 6,426 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
Recent reports of patient infection.
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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