American Contract Systems recalls 27 medical procedure kits due to unverified sterilization. Products may not meet sterilization standards, but no injuries reported. Check model numbers and lot numbers for affected items.
During an internal investigation, ACS determined that the rationale for sterilization of certain components was not justified and therefore, some components are not fit for further sterilization according to ACS procedures. As a result, ACS is unable to confirm product sterilization assurance requirements were met.
American Contract Systems is recalling 27 medical procedure kits and trays because some components were not properly sterilized. This means the products might not meet sterilization standards, but no injuries have been reported.
The recall states that during internal checks, American Contract Systems found that the sterilization process for some components wasn't properly justified. This means the products might not meet the required sterilization standards, but no injuries have been reported.
Healthcare professionals and medical facilities that use these kits are most at risk. The recall affects specific model numbers and lot numbers listed in the notice.
Check the model/serial numbers on the kit labels. Affected items include specific model numbers like ANCV78BC, ANVA82AB, and lot numbers such as 42-7844511.
Look for model numbers and lot numbers listed in the recall notice to determine if your kit is affected.
American Contract Systems determined that the sterilization process for some components wasn't properly justified, so the products may not meet sterilization standards.
The recall record states no injuries have been reported.
Check the model numbers and lot numbers listed in the recall notice, such as ANCV78BC with lot numbers 42-7844511.
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-2464-2025 — American Contract Systems American Contract Systems Hello, I own a American Contract Systems that is covered by recall Z-2464-2025 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.
