Olympus Tracheal Intubation Fiberscope recall
Olympus Tracheal Intubation Fiberscope, Models LF-P & LF-V.
Why was Olympus Tracheal Intubation Fiberscope recalled?
Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA 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?
UDI-DI: 04953170051098, 04953170452932, & 04953170156250; All Serial Numbers.
- Product
- Olympus Tracheal Intubation Fiberscope, Models LF-P & LF-V.
- Recalling firm
- Olympus Corporation of the Americas
- Quantity
- 2127 units
- Distribution
- US Nationwide distribution.
- Recall date
- September 6, 2023
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)