Bronchofiberscope BF-XP60
Reported: October 10, 2018 Initiated: August 8, 2018 #Z-3307-2018
Product Description
Bronchofiberscope BF-XP60
Reason for Recall
The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.
Details
- Recalling Firm
- Olympus Corporation of the Americas
- Units Affected
- 1296
- Distribution
- The products were distributed US nationwide and Canada.
- Location
- Center Valley, PA
Frequently Asked Questions
What product was recalled? ▼
Bronchofiberscope BF-XP60. Recalled by Olympus Corporation of the Americas. Units affected: 1296.
Why was this product recalled? ▼
The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to loosening of the instrument channel port.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on October 10, 2018. Severity: Moderate. Recall number: Z-3307-2018.
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