KNEE ARTHROSCOPY PACK-Procedure Kit Catalog Number: SFAR60A
FDA Recall #Z-2298-2024 — Class II — May 15, 2024
Product Description
KNEE ARTHROSCOPY PACK-Procedure Kit Catalog Number: SFAR60A
Reason for Recall
Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding component exceeded the residual limits for permanent exposure devices as indicated by ANSI/AAMI/ISO 10993-7/(R)2012.
Recalling Firm
American Contract Systems Inc — Tiffin, OH
Classification
Class II — May cause temporary or medically reversible adverse health consequences.
Product Type
Devices
Product Quantity
270 units
Distribution
US Nationwide distribution.
Code Information
UDI-DI: 00191072167408 LOT#"s: 992241 954241
Status
Ongoing
Voluntary / Mandated
Voluntary: Firm initiated