Class II
Medical Device Recall: Ivalon Eye Wick 20cm- Intended to be used for the removal and collection of fluids from the Opthalmic surgical site. Model Number: Q604206
Carwild Corporation · October 22, 2024
Reason for Recall
Potential for package seal to be out of specification and the sterile barrier cannot be guaranteed for the life of the product.
Distribution
IL, FL, SC. PA, AL Foreign: Netherlands
States Affected
AL, FL, IL, PA, SC
Quantity Affected
120 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-0798-2025
Status: ongoing
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