Olympus Pleuravideoscope, Model LTF-160
Reported: April 29, 2020 Initiated: March 23, 2020 #Z-1762-2020
Product Description
Olympus Pleuravideoscope, Model LTF-160
Reason for Recall
There was no data to validate that the identified endo-therapy devices were compatible with certain pleuravideoscope models. Updated Operations Manuals are being provided.
Details
- Recalling Firm
- Olympus Corporation of the Americas
- Units Affected
- 265 total
- Distribution
- US Nationwide
- Location
- Center Valley, PA
Frequently Asked Questions
What product was recalled? ▼
Olympus Pleuravideoscope, Model LTF-160. Recalled by Olympus Corporation of the Americas. Units affected: 265 total.
Why was this product recalled? ▼
There was no data to validate that the identified endo-therapy devices were compatible with certain pleuravideoscope models. Updated Operations Manuals are being provided.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on April 29, 2020. Severity: Moderate. Recall number: Z-1762-2020.
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