Recall
FDAHealthSeptember 11, 2025

Olympus Corporation of the Americas — EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE 1TQ180

⚠️ 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.

Is this relevant to me?

Geography
Nationwide
Source agency
FDA
Category
Health
Published
September 11, 2025

US Nationwide Distribution.

What's affected?

Product
EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE 1TQ180
Lot code
Model No. BF-1TQ180; UDI: 4953170339349; All Serial No.

Additional details

Model No. BF-1TQ180; UDI: 4953170339349; All Serial No.

What should I do?

Recommended action

Class I recall. Voluntary: Firm initiated Quantity affected: 215 units US; 736 units OUS.

View original FDA notice →

Get Health recall alerts

Delivered to your inbox. Free. No account required.