FDAFDA · Food and drugs·Recall number Z-2503-2023
Olympus Bronchovideoscope, Models BF-3C160.
Published September 6, 2023 · Recall initiated: July 27, 2023
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Olympus Corporation of the Americas
- Distributor
- US Nationwide distribution.
- Lot
- UDI-DI: 04953170340031 & 04953170063039; All Serial Numbers.
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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