Ivalon Eye Wick 20cm- Intended to be used for the removal and collection of fluids from the Opth...

FDA Recall #Z-0798-2025 — Class II — October 22, 2024

Recall #Z-0798-2025 Date: October 22, 2024 Classification: Class II Status: Ongoing

Product Description

Ivalon Eye Wick 20cm- Intended to be used for the removal and collection of fluids from the Opthalmic surgical site. Model Number: Q604206

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.

Recalling Firm

Carwild Corporation — New London, CT

Classification

Class II — May cause temporary or medically reversible adverse health consequences.

Product Type

Devices

Product Quantity

120 units

Distribution

IL, FL, SC. PA, AL Foreign: Netherlands

Code Information

LOT NUMBER: 24G1880

Status

Ongoing

Voluntary / Mandated

Voluntary: Firm initiated