Olympus Bronchofiberscope BF Type recalled for combustion risk during laser procedures
Olympus bronchoscopes (Models BF-PE2 and BF-TE2) are recalled due to reports of combustion inside the airway during laser-assisted medical procedures. This is an FDA Class I recall.
- Product
- Olympus BRONCHOFIBERSCOPE BF Type, Model Numbers BF-PE2, BF-TE2
- Category
- Medical Device
- Distribution
- Distributed nationwide