FDA-Device2023-09-06Class II
EVIS EXERA III DUODENOVIDEOSCOPE OLYMPUS TJF-Q190V
Hazard
Recent reports of patient infection.
Sold states
US Nationwide distribution.
Affected count
6,426 units
Manufactured in
3500 Corporate Pkwy, N/A, Center Valley, PA, United States
Products
EVIS EXERA III DUODENOVIDEOSCOPE OLYMPUS TJF-Q190V
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2467-2023More Olympus Corporation of the Americas recalls
- FDA-Device2026-04-08Olympus SOLTIVE Premium laser system recalled for defective power supply
- FDA-Device2026-04-08Olympus SOLTIVE Pro SuperPulsed Laser System recalled for power supply defect
- FDA-Device2026-04-01Olympus PKS Cutting Forceps recalled for defective welds causing jaw breakage
- FDA-Device2026-04-01Olympus MAJ-1443 and MAJ-1444 endoscope suction valves no longer compatible with OER-Pro and OER-Elite reprocessors
- FDA-Device2026-04-01Olympus PKS Cutting Forceps recalled for defective welds causing jaw breakage
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