American Contract Systems recalls LAPAROSCOPY PACK models LLLA21J and LLLA21J-02 due to possible sterilization issues affecting medical use safety.
ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
American Contract Systems is recalling LAPAROSCOPY PACKs with specific model numbers because they may not have been properly sterilized. This could lead to delays or longer medical procedures if the equipment isn't functioning correctly.
The equipment may not have been properly sterilized, which could lead to contamination. This might cause the device to malfunction during surgery, potentially delaying or prolonging treatment.
Medical professionals using the recalled LAPAROSCOPY PACKs for surgical procedures are most at risk. Patients undergoing surgery with these devices may experience treatment delays or extended procedures.
Check for model numbers LLLA21J or LLLA21J-02 on the packaging. The product was sold with specific lot numbers: 882241, 70-051163, 70-051373, 70-051564, 70-052582, and 70-053048.
Look for model numbers LLLA21J or LLLA21J-02 on the packaging or product.
American Contract Systems is unable to confirm that the product met sterilization assurance requirements, which could lead to delays or prolonged treatment.
The recall does not specify a remedy, so check the model numbers and lot numbers to determine if your product is affected.
The recall states possible loss or lack of functionality may lead to delays or prolonged treatment, but does not mention serious injury risks.
We’ve drafted a message you can send American Contract Systems to request your refund or repair — edit it as you like.
Subject: Recall Z-1337-2025 — American Contract Systems American Contract Systems Hello, I own a American Contract Systems that is covered by recall Z-1337-2025 from American Contract Systems. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
