Carefusion recalls Genesis STERRAD reusable 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 STERRAD reusable sterilization containers because they did not consistently pass aerosol challenge testing. This means the containers might not seal properly during use, potentially leading to contamination of medical equipment.
These containers are designed to be reused for sterilizing medical equipment. If they don't seal properly during use, they may allow contaminants to enter the sterilization process, potentially leading to infections.
Healthcare facilities using these containers for medical sterilization are most at risk. Patients and staff could be exposed to contaminants if the containers fail to seal properly.
Check for the model: Genesis FULL-LENGTH CONTAINER 23 X12" (58.4 X 30.5CM) 5" (12.7CM) DEEP STERRAD COMPATIBLE. The lot numbers start with UDI/DI (01) 10885403019357.
Identify the model number on the container to confirm it matches the recalled Genesis STERRAD Full-Length Container.
The containers did not consistently meet requirements for aerosol challenge testing, which means they may not seal properly during use.
Look for the model: Genesis FULL-LENGTH CONTAINER 23 X12" (58.4 X 30.5CM) 5" (12.7CM) DEEP STERRAD COMPATIBLE with lot numbers starting with UDI/DI (01) 10885403019357.
The recall record does not specify a remedy, so contact Carefusion for guidance.
We’ve drafted a message you can send Carefusion to request your refund or repair — edit it as you like.
Subject: Recall Z-0213-2023 — Carefusion Carefusion Hello, I own a Carefusion that is covered by recall Z-0213-2023 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.
