Laparoscopy Pack (American Contract) – sterilization uncertainty (2025)
Hazard assessment based on recall description.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
LAPAROSCOPY PACK, Model Nos LLLA21J LLLA21J-02
Brand
American Contract Systems Inc
Lot Codes / Batch Numbers
UDI-DI 00191072219206 Lots 882241 70-051163 70-051373 70-051564 70-052582 70-053048
Products Sold
UDI-DI 00191072219206 Lots 882241 70-051163 70-051373 70-051564 70-052582 70-053048
American Contract Systems Inc is recalling LAPAROSCOPY PACK, Model Nos LLLA21J LLLA21J-02 due to ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged . Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
Recommended Action
Per FDA guidance
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.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026