Olympus Pleuravideoscope recall
Olympus Pleuravideoscope, Model LTF-160
Why was Olympus Pleuravideoscope 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.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
All Serial numbers
- Product
- Olympus Pleuravideoscope, Model LTF-160
- Recalling firm
- Olympus Corporation of the Americas
- Quantity
- 265 total
- Distribution
- US Nationwide
- Recall date
- April 29, 2020
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)