Olympus Corporation of the Americas recalls OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE P60

Recall date

September 11, 2025

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-0058-2026

FDA classification

Class I

Brand / firm

Olympus Corporation of the Americas

Sold / distributed

US Nationwide Distribution.

Why it was recalled

Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency therapy equipment.

Class I is the FDA’s most serious recall level: there is a reasonable probability that using this product will cause serious harm or death.

What was recalled

OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE P60