CAREFUSION extension sets with specific model numbers may have flow issues leading to therapy delays. Affected products include BD Extension Sets SMALLBORE Tubing SmartSite VALVE and related items. Contact CAREFUSION for details.
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 recalls certain extension sets that may cause flow issues, leading to therapy delays. This affects medical devices used for treatments like IV therapy. Users should check their product model numbers to see if they are affected.
The needle-free connector valves in these extension sets may have difficulty flushing or flow issues, which can cause partial or total blockages. This could lead to therapy delays if the device is not functioning properly.
Patients using IV therapy or similar medical treatments with the recalled extension sets are most at risk. Healthcare providers and patients who own the affected models should check their product details.
Check for model numbers like 10010511, 10010912, or 20035E on the product. The recall includes specific extension sets used in medical treatments.
Look for model numbers such as 10010511, 10010912, or 20035E on the extension set.
No, the recall does not require stopping use. The products may have flow issues but do not pose an immediate risk of injury.
Check the model number on your extension set. Affected models include 10010511, 10010912, and others listed in the recall notice.
Contact CAREFUSION directly for instructions on how to handle the affected product. The recall does not specify a replacement or return process.
We’ve drafted a message you can send CAREFUSION to request your refund or repair — edit it as you like.
Subject: Recall Z-2460-2021 — CAREFUSION CAREFUSION Hello, I own a CAREFUSION that is covered by recall Z-2460-2021 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.
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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.
