Carwild Ivalon CELLULOSE SURGICAL SPEAR- Intended To Be Used During Ophthalmic Surgical recall — FDA Z-0799-2025
Potential for package seal to be out of specification and the sterile barrier cannot be guaranteed for the life of the product.
Overview of recall records associated with Carwild Corporation, including dates, categories and classifications where available.
Classification mix: Class II: 3.
Potential for package seal to be out of specification and the sterile barrier cannot be guaranteed for the life of the product.
Potential for package seal to be out of specification and the sterile barrier cannot be guaranteed for the life of the product.
Potential for package seal to be out of specification and the sterile barrier cannot be guaranteed for the life of the product.
This page summarizes recall records in which the official source identifies Carwild Corporation as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.