FDA-Device2023-09-06Class II
Olympus Tracheal Intubation Fiberscope, Models LF-P & LF-V.
Hazard
Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.
Sold states
US Nationwide distribution.
Affected count
2127 units
Manufactured in
3500 Corporate Pkwy, N/A, Center Valley, PA, United States
Products
Olympus Tracheal Intubation Fiberscope, Models LF-P & LF-V.
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2501-2023More 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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