American Contract Systems recalls D&C packs with unvalidated sterilization cycles. Affected items have specific tray, lot, and serial numbers. Stop using if you have these items.
Product was exposed to multiple sterilization cycles without validation for multiple exposures.
American Contract Systems is recalling D&C packs that were exposed to multiple sterilization cycles without proper validation. This could lead to improper sterilization and potential infection risks if the packs are used.
The packs were sterilized multiple times without validation, meaning the sterilization process wasn't confirmed to work correctly. This could result in the packs not being sterile when used, increasing infection risk during medical procedures.
Healthcare workers using D&C packs for medical procedures are most at risk. Patients using these packs could face infection if the packs are not properly sterilized.
Check for the tray number LLDC40G, sterilization lot 2108101, lot number 785211, and bag serial number 44272963-005 on the D&C pack.
Look for the tray number LLDC40G, sterilization lot 2108101, lot number 785211, and bag serial number 44272963-005 on the D&C pack.
The recalled D&C pack has tray number LLDC40G, sterilization lot 2108101, lot number 785211, and bag serial number 44272963-005.
The packs were exposed to multiple sterilization cycles without validation, which could lead to improper sterilization and infection risks.
The recall does not specify a stop-use instruction, so you can continue using them if you don't have the specific serial numbers listed.
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-1704-2022 — American Contract Systems American Contract Systems Hello, I own a American Contract Systems that is covered by recall Z-1704-2022 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.
