American Contract Systems recalls LABOR & DELIVERY PPS models LLLD64O-01, -02 due to possible sterilization issues affecting medical use. No remedy specified in recall notice.
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 certain LABOR & DELIVERY PPS models because they may not have been properly sterilized, which could delay or prolong medical treatment. This is a medical device recall that requires attention to ensure patient safety.
The devices may not meet sterilization requirements, which could lead to contamination or infection risks during medical procedures. This might cause delays or extended treatment times for patients.
Healthcare providers using the LABOR & DELIVERY PPS models in medical settings are likely affected. Patients receiving treatment with these devices could be at risk if sterilization is compromised.
Check for model numbers LLLD64O-01, LLLD64O-02 on the device. The recall includes specific production lots: 892241, 70-051048, 70-051516, 70-052113, 70-052313, 70-052401, 70-052911.
Look for model numbers LLLD64O-01 or LLLD64O-02 on the device.
The recall is due to possible failure to meet sterilization requirements, which could lead to delays or prolonged treatment.
The recall notice does not specify a remedy, so no action is required beyond checking if your device is affected.
Yes, the recall includes production lots: 892241, 70-051048, 70-051516, 70-052113, 70-052313, 70-052401, 70-052911.
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-1344-2025 — American Contract Systems American Contract Systems Hello, I own a American Contract Systems that is covered by recall Z-1344-2025 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.
