Olympus BRONCHOFIBERSCOPE BF Type, Model Numbers BF-PE2, BF-TE2
Reported: July 26, 2023 Initiated: June 8, 2023 #Z-2012-2023
Product Description
Olympus BRONCHOFIBERSCOPE BF Type, Model Numbers BF-PE2, BF-TE2
Reason for Recall
There have been complaints of endobronchial combustion during therapeutic laser procedures with the bronchoscope.
Details
- Recalling Firm
- Olympus Corporation of the Americas
- Units Affected
- 4 units
- Distribution
- US Nationwide Distribution.
- Location
- Center Valley, PA
Frequently Asked Questions
What product was recalled? ▼
Olympus BRONCHOFIBERSCOPE BF Type, Model Numbers BF-PE2, BF-TE2. Recalled by Olympus Corporation of the Americas. Units affected: 4 units.
Why was this product recalled? ▼
There have been complaints of endobronchial combustion during therapeutic laser procedures with the bronchoscope.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on July 26, 2023. Severity: Critical. Recall number: Z-2012-2023.
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