American Contract Systems recalls General Laparoscopic Pack-LF models UTGL53S-06-08 due to possible failure in sterilization assurance, which could delay or prolong medical treatments.
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 specific laparoscopic surgical packs because they may not have been properly sterilized. This could lead to delays or longer treatment times for patients needing surgery.
The packs may not meet sterilization requirements, which could cause delays or extended treatment periods during surgery. This is a risk to patient care but does not involve immediate physical harm.
Surgical teams and hospitals using the recalled laparoscopic packs. Patients undergoing surgery are at risk if the packs are not properly sterilized.
Check for model numbers UTGL53S-06, UTGL53S-07, or UTGL53S-08 on the pack. The packs were sold with specific lot numbers including 941241, 899241, 70-050873, 70-051230, 70-051578, and 70-052009A.
Identify the model number on the pack to confirm if it is one of UTGL53S-06, UTGL53S-07, or UTGL53S-08.
Reach out to American Contract Systems for guidance on next steps if the product is recalled.
American Contract Systems cannot confirm that the packs met sterilization requirements, which could lead to delays or prolonged treatment.
Check the model number and contact American Contract Systems for guidance on next steps.
The recall is due to possible failure in sterilization assurance, which could delay or prolong medical treatments but does not involve immediate health 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-1357-2025 — American Contract Systems American Contract Systems Hello, I own a American Contract Systems that is covered by recall Z-1357-2025 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.
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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.
