CAREFUSION recalls specific infusion burette sets that may have flow problems, leading to therapy delays. Check your product details to see if you're affected.
Needle-free connector valves, either standalone or attached to extension sets, may have issues including difficulty to flush, flow issues, and partial or total occlusions, which could lead to therapy delay. Follow-up activates not required if product has already been used or was safely connected to the female luer of connecting device.
CAREFUSION is recalling certain infusion burette sets that may cause flow issues, leading to therapy delays. This could affect patients using these devices for medical treatments.
The needle-free connector valves in these sets may have issues like difficulty flushing, flow problems, or partial or total blockages. This could delay medical therapy if the device isn't functioning properly.
People using CAREFUSION infusion burette sets for medical treatments are likely affected. Those with specific model numbers or lot codes listed in the recall are at higher risk.
Check for model numbers like 10015012, 10817920, or lot codes such as 20055717 listed in the recall. These sets are used with CAREFUSION pumps for medical infusion therapy.
Review your product's model number or lot code to see if it matches the recalled items listed in the recall notice.
No, the recall does not require immediate stop use. However, you should check if your product is affected and take action if needed.
The recall does not specify a remedy, so you should check the product details to see if it's affected and contact CAREFUSION for further instructions.
Look for model numbers like 10015012, 10817920, or lot codes such as 20055717 listed in the recall notice.
We’ve drafted a message you can send CAREFUSION to request your refund or repair — edit it as you like.
Subject: Recall Z-2459-2021 — CAREFUSION CAREFUSION Hello, I own a CAREFUSION that is covered by recall Z-2459-2021 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
