OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE 1T60
Reported: October 22, 2025 Initiated: September 11, 2025 #Z-0047-2026
Product Description
OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE 1T60
Reason for Recall
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.
Details
- Recalling Firm
- Olympus Corporation of the Americas
- Units Affected
- 347 units US; 2,869 units OUS
- Distribution
- US Nationwide Distribution.
- Location
- Center Valley, PA
Frequently Asked Questions
What product was recalled? ▼
OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE 1T60. Recalled by Olympus Corporation of the Americas. Units affected: 347 units US; 2,869 units OUS.
Why was this product 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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on October 22, 2025. Severity: Critical. Recall number: Z-0047-2026.
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