Recalls / —
—#212719
Product
C-SECTION PPS , Model No LLCI66M LLCI66M-02 LLCI66M-03 LLCI66M-04
- FDA product code
- OHM — Cesarean Section Tray
- Device class
- Class 2
- Medical specialty
- Obstetrics/Gynecology
- Affected lot / code info
- UDI-DI 00191072219596 Lots 907241 70-050816 70-051301 70-051839 70-052420 70-052910 70-053100
Why it was recalled
ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
Root cause (FDA determination)
Process control
Action the firm took
The affected distributor was notified via email on 2/16/25, and an updated letter was provided on 2/18/25. The distributor was instructed to notify their end users. Customers were provided with a list of impacted components which are included in the affected trays. Customers were provided with a labeling template and instructed to add warning labels to affected procedure trays to ensure the affected components are discarded.
Recalling firm
- Firm
- American Contract Systems Inc
- Address
- 85 Shaffer Park Dr, Tiffin, Ohio 44883-9290
Distribution
- Distribution pattern
- US Nationwide distribution in the state of OH.
Timeline
- Recall initiated
- 2025-02-06
- Posted by FDA
- 2025-03-14
- Status
- —
Source: openFDA Device Recall endpoint. Recall record ID #212719. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.