Model No. ENF-XP recall
Model No. ENF-XP, RHINO-LARYNGOFIBERSCOPE
Why was Model No. ENF-XP recalled?
Olympus has updated the instructions for use: Reusable cleaning brushes have been removed from the manual cleaning. Single use brushes remain compatible.
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: 04953170059018 All serial numbers
- Product
- Model No. ENF-XP, RHINO-LARYNGOFIBERSCOPE
- Recalling firm
- Shirakawa Olympus Co., Ltd.
- Quantity
- 1929 US; 2200 OUS
- Distribution
- US Nationwide distribution.
- Recall date
- January 17, 2024
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)