CAREFUSION recalls Gravity Burette Set 60 DP 3 SmartSite Valves due to potential flow issues and occlusions that may delay therapy. Affected units include specific lot numbers.
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 its Gravity Burette Set 60 DP 3 SmartSite Valves because they may cause flow problems or blockages, leading to therapy delays. This affects users who rely on these valves for medical treatments.
The valves may have difficulty flushing or flow issues, causing partial or total blockages. This can delay therapy but does not pose an immediate risk of injury or serious harm.
Users of the Gravity Burette Set 60 DP 3 SmartSite Valves for medical therapy are most at risk. This includes patients using the product for treatment purposes.
Check for the product name 'Gravity Burette Set 60 DP 3 SmartSite Valves' and lot numbers 20026597, 20026598, 20096477, 20106218, 20115237, or 20126022, 20126023.
Identify the lot numbers from the list: 20026597, 20026598, 20096477, 20106218, 20115237, 20126022, 20126023.
No, the recall does not require immediate discontinuation. The valves may still be used safely if they function properly.
The official recall does not specify a remedy, so contact CAREFUSION directly for guidance.
The recall states the valves may cause therapy delays but does not mention 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-2462-2021 — CAREFUSION CAREFUSION Hello, I own a CAREFUSION that is covered by recall Z-2462-2021 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.
