Ivalon Eye Wick 20cm- Intended to be used for the recall: Sterility Concern
Ivalon Eye Wick 20cm- Intended to be used for the removal and collection of fluids from the Opthalmic surgical site. Model Number: Q604206
Why was Ivalon Eye Wick 20cm- Intended to be used for the recalled?
Potential for package seal to be out of specification and the sterile barrier cannot be guaranteed for the life of the product.
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?
LOT NUMBER: 24G1880
- Product
- Ivalon Eye Wick 20cm- Intended to be used for the removal and collection of fluids from the Opthalmic surgical site. Model Number: Q604206
- Recalling firm
- Carwild Corporation
- Quantity
- 120 units
- Distribution
- IL, FL, SC. PA, AL Foreign: Netherlands
- Recall date
- January 8, 2025
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)