Carefusion recalls Genesis mid-length sterilization containers that failed aerosol challenge testing. These containers may not properly seal during use, risking contamination. Affected units have specific model and lot numbers.
Genesis STERRAD Reusable Rigid Sterilization Containers have not consistently met the requirements for aerosol challenge testing.
Carefusion is recalling Genesis mid-length sterilization containers that didn't consistently pass aerosol testing. This means the containers might not seal properly during use, potentially leading to contamination risks.
These containers failed aerosol challenge testing, meaning they may not seal properly during use. This could allow contaminants to enter the container, risking infection if used for medical purposes.
Users of medical sterilization containers for healthcare settings. Healthcare workers handling these containers are most at risk.
Check for the model name 'Genesis MID-LENGTH CONTAINER 19X12" (48.3 X 30.5CM) 4" (10CM) DEEP STERRAD COMPATIBLE, REF CD2-4ST'. All units with UDI/DI (01) 10885403019111 are affected.
Identify the model number on the container to confirm if it matches the recalled version.
Reach out to Carefusion for specific guidance on handling affected containers.
The containers failed aerosol challenge testing, meaning they may not seal properly during use, potentially allowing contamination.
No immediate stop is required; the recall is for replacement or further evaluation by the manufacturer.
Check the model number and contact Carefusion for specific instructions on handling affected units.
We’ve drafted a message you can send Carefusion to request your refund or repair — edit it as you like.
Subject: Recall Z-0208-2023 — Carefusion Carefusion Hello, I own a Carefusion that is covered by recall Z-0208-2023 from Carefusion. 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.
