FDAFDA · Food and drugs·Recall number Z-3288-2018
Bronchovideoscope F-1TQ180
Published October 10, 2018 · Recall initiated: August 8, 2018
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
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.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Olympus Corporation of the Americas
- Distributor
- The products were distributed US nationwide and Canada.
- Lot
- all lot codes
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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