Carefusion recalls Genesis Mini Sterilization Containers due to inconsistent aerosol challenge testing. Affected units have specific dimensions and UDI codes. Consumers should contact Carefusion for details.
Genesis STERRAD Reusable Rigid Sterilization Containers have not consistently met the requirements for aerosol challenge testing.
Carefusion is recalling Genesis Mini Sterilization Containers because they didn't consistently pass aerosol challenge testing. This could mean the containers might not properly seal during sterilization, risking contamination of medical equipment.
These containers are designed to hold surgical instruments during sterilization. If they don't consistently pass aerosol challenge testing, they might not seal properly, potentially allowing contaminants to enter the sterilization process.
Healthcare facilities using these containers for medical sterilization are most likely affected. Patients and staff using the containers for surgical instruments may be at risk if the containers fail to seal properly.
Check for the container dimensions: 10-1/2 X 7-1/2" (26.7X19.0CM) with a 3" (7.6CM) depth. The UDI code 10885403018886 is listed for all lots. The product name includes 'Genesis STERRAD Reusable Rigid Sterilization Containers'.
Verify the container dimensions and UDI code to confirm if your unit is affected.
The containers did not consistently meet the requirements for aerosol challenge testing, which could affect their ability to seal properly during sterilization.
Look for the specific dimensions (10-1/2 X 7-1/2" (26.7X19.0CM) with 3" (7.6CM) depth) and UDI code 10885403018886 on the container.
Contact Carefusion directly for further instructions as the recall remedy is not specified in the record.
We’ve drafted a message you can send Carefusion to request your refund or repair — edit it as you like.
Subject: Recall Z-0203-2023 — Carefusion Carefusion Hello, I own a Carefusion that is covered by recall Z-0203-2023 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.
