American Contract Systems recalls three convenience kits that may not have been properly sterilized due to insufficient aeration time during use. Affected kits include specific models and lots with expiration dates through January 2025.
Product released with insufficient aeration time impacting the kits sterilized on the same cycle or in the same aeration chamber, which may have been compromised in sterility
American Contract Systems is recalling three convenience kits that may have been compromised in sterility because they were sterilized with insufficient aeration time. This could lead to contamination risks if used for medical purposes.
The kits may not have been properly sterilized during the aeration cycle, which could lead to contamination. This happens because the sterilization process requires sufficient aeration time to ensure the kits are safe for medical use.
Users of these medical convenience kits, particularly those in healthcare settings or home medical care, may be affected. The risk is low as the kits are designed for specific medical use cases.
Check for model numbers: ALEX17A, AKHD97A, or CETJ13O. The kits were sold with specific lot numbers and expiration dates through January 2025.
Identify the model number and lot number on the kit to confirm if it is affected.
The kits may have been compromised in sterility due to insufficient aeration time, so they should not be used until the recall is addressed.
Check the model number and lot number to see if it is affected; if so, stop using it and contact American Contract Systems for further instructions.
Affected kits have model numbers ALEX17A, AKHD97A, or CETJ13O with specific lot numbers and expiration dates through January 2025.
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-2521-2024 — American Contract Systems American Contract Systems Hello, I own a American Contract Systems that is covered by recall Z-2521-2024 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.
