Carefusion recalls Genesis mid-length sterilization containers that failed aerosol challenge testing. These containers may not meet safety standards for sterilization processes.
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 did not consistently pass aerosol challenge testing. This means the containers might not meet safety standards for sterilization processes, potentially affecting medical procedures.
These containers failed to consistently meet aerosol challenge testing requirements. This means they might not properly maintain sterility during medical sterilization processes, potentially leading to contamination risks.
Healthcare facilities using these containers for medical sterilization are likely affected. Patients and staff at facilities using the recalled containers face the lowest risk of harm.
Check for the model: Genesis mid-length container 19X12" (48.3 X 30.5CM) 5" (12.7CM) deep STERRAD compatible. The recall includes all lots with UDI/DI (01) 10885403019142.
Identify the model and lot number to confirm if your container is recalled.
The recall indicates these containers did not consistently pass aerosol challenge testing, so they may not meet safety standards for sterilization.
The recall does not specify a remedy, so check with Carefusion for guidance on next steps.
Look for the model: Genesis mid-length container 19X12" (48.3 X 30.5CM) 5" (12.7CM) deep STERRAD compatible with UDI/DI (01) 10885403019142.
We’ve drafted a message you can send Carefusion to request your refund or repair — edit it as you like.
Subject: Recall Z-0209-2023 — Carefusion Carefusion Hello, I own a Carefusion that is covered by recall Z-0209-2023 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.
