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Carwild Corporation recalls Ivalon Eye Wick 20cm- Intended to be used for the removal and collection of fluids from the Opthalmic surgical site.
Recalled January 8, 2025 · FDA recall Z-0798-2025 · Carwild
Hazard
Potential for package seal to be out of specification and the sterile barrier cannot be guaranteed for the life of the product. · FDA Class II
Units
120 units
Sold at
IL, FL, SC. PA, AL Foreign: Netherlands
Description
Potential for package seal to be out of specification and the sterile barrier cannot be guaranteed for the life of the product.
Product
Ivalon Eye Wick 20cm- Intended to be used for the removal and collection of fluids from the Opthalmic surgical site. Model Number: Q604206
Manufacturer(s)
Carwild Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →