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.
- Class II: Risk 09/04/2025
- Class II: Risk 09/04/2025
- Class II: Risk 09/04/2025
- Class II: Risk 09/04/2025
- Class II: Risk 09/04/2025
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.