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 its Genesis mid-length sterilization containers because they failed 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 could allow contaminants to enter the sterilization process, potentially causing infections.
Healthcare facilities using these containers for medical sterilization are most affected. Patients and staff using the containers for procedures may be at risk if the containers fail to seal properly.
Check for the model: Genesis mid-length container 19X12" (48.3 X 30.5CM) 6" (15.2CM) deep STERRAD compatible. The specific lot numbers include UDI/DI (01) 10885403019173.
Look for the model number on the container: Genesis mid-length container 19X12" (48.3 X 30.5CM) 6" (15.2CM) deep STERRAD compatible.
The containers failed aerosol challenge testing, meaning they may not seal properly during use and could lead to contamination of medical equipment.
The recall does not require immediate stoppage; however, healthcare facilities should check their containers and follow the provided steps.
The recall does not specify a remedy, so contact Carefusion for guidance on next steps.
We’ve drafted a message you can send Carefusion to request your refund or repair — edit it as you like.
Subject: Recall Z-0210-2023 — Carefusion Carefusion Hello, I own a Carefusion that is covered by recall Z-0210-2023 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.
