American Contract Systems Inc: Device Recall
Recall #Z-2465-2025 · 07/14/2025
Class II: Risk
Recall Details
- Recall Number
- Z-2465-2025
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- American Contract Systems Inc
- Status
- Ongoing
- Date Initiated
- 07/14/2025
- Location
- Tiffin, OH, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 1233 units
Reason for Recall
During an internal investigation, ACS determined that the rationale for sterilization of certain components was not justified and therefore, some components are not fit for further sterilization according to ACS procedures. As a result, ACS is unable to confirm product sterilization assurance requirements were met.
Product Description
AMERICAN CONTRACT SYSTEMS, Medical Procedure kits and trays labeled as: 1) LAP CHOLE PACK, Model/Item Number CILC69L; 2) LAP CHOLE PACK, Model/Item Number HNLC80J; 3) LAP CHOLE PACK, Model/Item Number JKLC55H; 4) LAPAROSCOPY PACK, Model/Item Number LLLA21K; 5) GENERAL LAPAROSCOPY MPH, Model/Item Number MPGL15G;
Distribution Pattern
US distribution to states of: IL and LA
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.