Steris recalls Verify SixCess Challenge Pack due to incorrect chemical indicators in packaging. Affected units have UDI-DI 1072499:5088955 and item number LCC003, lot 3411228A.
Product contains incorrect chemical indicators in packaging.
Steris is recalling Verify SixCess Challenge Packs because they contain incorrect chemical indicators in the packaging. This could lead to improper steam sterilization verification, potentially affecting medical safety.
The chemical indicators in the packaging are incorrect, which means the packs may not properly show when steam sterilization has reached critical parameters. This could lead to improper sterilization verification in medical settings.
Healthcare facilities using Verify SixCess Challenge Packs for steam sterilization testing are likely affected. Users must check if their packs have the specific UDI-DI and item number listed.
Check for the UDI-DI number 10724995088955 and item number LCC003 on the packaging. The affected lot number is 3411228A.
Look for the UDI-DI number 10724995088955 and item number LCC003 on the packaging.
The affected lot number is 3411228A.
Check for the UDI-DI number 10724995088955 and item number LCC003 on the packaging. The affected lot number is 3411228A.
The recall record does not specify a remedy.
We’ve drafted a message you can send Steris to request your refund or repair — edit it as you like.
Subject: Recall Z-1736-2022 — Steris Steris Hello, I own a Steris that is covered by recall Z-1736-2022 from Steris. 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.
