Recall of American Contract Systems Hand Pack convenience kits due to potential sterility compromise from insufficient aeration time during sterilization cycles.
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 hand pack convenience kits because they may not have been properly sterilized due to insufficient aeration time. This could lead to contamination risks if used for medical purposes.
The kits may not have been properly sterilized because the aeration time was too short during the sterilization cycle. This could allow contaminants to remain in the kit, potentially causing infections if used for medical purposes.
Users of the American Contract Systems Hand Pack convenience kits, particularly those using them for medical sterilization. Healthcare facilities and medical professionals handling these kits are most at risk.
Check for the UDI-DI number 00191072203717, Lot 982241, and expiration date 1/18/2025 on the kit packaging.
Verify the UDI-DI number 00191072203717, Lot 982241, and expiration date 1/18/2025 on the kit.
American Contract Systems is recalling Hand Pack convenience kits due to potential sterility issues from insufficient aeration time during sterilization cycles.
Check for the UDI-DI number 00191072203717, Lot 982241, and expiration date 1/18/2025 on the kit packaging.
The recall record does not specify a remedy, so no action is required beyond checking the kit details.
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-2517-2024 — American Contract Systems American Contract Systems Hello, I own a American Contract Systems that is covered by recall Z-2517-2024 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.
