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FDAFDA · Food and drugs·Recall number Z-2285-2024

FOOT ANKLE-LF Procedure tray Catalog Number:CCFA51B

Published July 17, 2024 · Recall initiated: May 15, 2024

Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the hazard

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.

What to do

Voluntary: Firm initiated · E-Mail

Recall details

Manufacturer
American Contract Systems Inc
Distributor
US Nationwide distribution.
Lot
UDI-DI: 00191072193148 LOT#"s: 651231 983241 940241 901241
Risk classification
Class II
Area (FDA)
device
Country
United States

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