FDAFDA · Food and drugs·Recall number Z-1762-2020
Olympus Pleuravideoscope, Model LTF-160
Published April 29, 2020 · Recall initiated: March 23, 2020
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
There was no data to validate that the identified endo-therapy devices were compatible with certain pleuravideoscope models. Updated Operations Manuals are being provided.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Olympus Corporation of the Americas
- Distributor
- US Nationwide
- Lot
- All Serial numbers
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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