CAREFUSION recalls BD SmartSite needle-free valve products due to potential flow issues and occlusions that could delay therapy. Affected items include specific model numbers and lots listed in the recall notice.
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 several SmartSite needle-free valve products that may have flow issues, causing therapy delays. This is due to problems with the connector valves that could lead to partial or total blockages.
The needle-free connector valves in the recalled products may have difficulty flushing or flow issues, leading to partial or total blockages. This could cause therapy delays but does not pose an immediate risk of serious injury.
Users of the recalled SmartSite needle-free valve products, particularly those in medical settings using these devices for therapy. Patients and healthcare providers who have the affected models are most at risk.
Check for the product names and model numbers listed in the recall notice, including BD SmartSite, Connector, J-LOOP Extension Set, and other specific valve models with the referenced lot numbers.
Review the product names and model numbers listed in the recall notice to confirm if your item is affected.
No, the recall does not require immediate discontinuation. The products may still be used safely if they have been properly connected to the female luer of a connecting device.
The recall notice does not specify a remedy, so no action is required beyond checking if your product is listed.
The recall states that the products may cause therapy delays due to flow issues, but there is no mention of serious injury risks.
We’ve drafted a message you can send CAREFUSION to request your refund or repair — edit it as you like.
Subject: Recall Z-2467-2021 — CAREFUSION CAREFUSION Hello, I own a CAREFUSION that is covered by recall Z-2467-2021 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.
