American Contract Systems recalls C-SECTION PACK models LLCS44F and LLCS44F-01 due to possible sterilization issues causing treatment delays. Affected units sold with specific lot numbers.
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 C-SECTION PACK surgical products with model numbers LLCS44F and LLCS44F-01 because they may not have been properly sterilized. This could lead to delays or extended treatment times for patients needing these products.
The products may not have been properly sterilized, which could result in contamination. This might cause treatment delays or longer procedures if the products don't function as expected.
Surgical staff and patients using the recalled C-SECTION PACK products for procedures. Those most at risk are healthcare providers handling the products during surgeries.
Check for model numbers LLCS44F or LLCS44F-01 on the product. Affected units were sold with specific lot numbers: 70-051011, 70-051709, 70-052452, and 70-052952.
Look for model numbers LLCS44F or LLCS44F-01 on the C-SECTION PACK.
American Contract Systems cannot confirm that the products were properly sterilized, which may cause treatment delays or prolonged procedures.
The recall record does not specify a remedy, so no action is required beyond checking if the product matches the model numbers and lot numbers listed.
The recall indicates possible treatment delays or extended procedures, but no specific safety risks like injury are mentioned.
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-1336-2025 — American Contract Systems American Contract Systems Hello, I own a American Contract Systems that is covered by recall Z-1336-2025 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.
