American Contract Systems, Inc.: Device Recall

Recall #Z-1916-2025 · 04/21/2025

Class II: Risk

Recall Details

Recall Number
Z-1916-2025
Classification
Class II
Product Type
Device
Recalling Firm
American Contract Systems, Inc.
Status
Ongoing
Date Initiated
04/21/2025
Location
Chandler, AZ, United States
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
850 Kits

Reason for Recall

Test results for cast padding component included in procedure trays shows Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals exceeded residual limits, which may lead to a possible loss or lack of functionality that may lead to a delay or prolonged treatment/procedure/therapy.

Product Description

LOWER EXTREMITY, Model: NCEX20I; LOWER EXTREMITY, Model: NCEX20J; TOTAL KNEE PACK, Model: NCTK31K; TOTAL KNEE PACK, Model: NCTK31L All convenience kits contain Specialist Blend Cast Padding, Item: QTX30-322NS

Distribution Pattern

US Nationwide distribution in the state of CO.

Other Recalls by American Contract Systems, Inc.

View all recalls by American Contract Systems, Inc. →

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.