Carefusion recalls Genesis STERRAD reusable sterilization containers that failed aerosol challenge testing. These containers may not meet safety standards for sterilization.
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 could mean the containers may not meet safety standards for sterilization, potentially affecting medical procedures.
The containers did not consistently meet requirements for aerosol challenge testing. This means they might not properly sterilize medical instruments, increasing the risk of infection during procedures.
Healthcare facilities using Carefusion Genesis STERRAD containers are likely affected. Patients undergoing procedures with these containers may be at risk if the containers fail to meet sterilization standards.
Check for the model: Genesis STERRAD Full-Length Container 23 X12" (58.4 X 30.5CM) 7" (17.8CM) DEEP, Perforated. The unique identifier is UDI/DI (01) 10885403019432 across all lots.
Look for the model number and unique identifier (UDI/DI 10885403019432) on the container.
The containers did not consistently meet requirements for aerosol challenge testing, which could affect sterilization safety.
Check for the model: Genesis STERRAD Full-Length Container 23 X12" (58.4 X 30.5CM) 7" (17.8CM) DEEP, Perforated with UDI/DI (01) 10885403019432 across all lots.
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-0215-2023 — Carefusion Carefusion Hello, I own a Carefusion that is covered by recall Z-0215-2023 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.
