CAREFUSION recalls BD SE Burette Set 20 Drops 2 Injection Ports with flow issues that may cause therapy delays. Affected lots listed; no remedy specified in official 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 BD SE Burette Set 20 Drops 2 Injection Ports due to potential flow issues that could delay therapy. This affects specific production lots. The recall does not include a remedy.
The needle-free connector valves in the set may have difficulty flushing or flow issues, leading to partial or total blockages. This could delay therapy if the device is not functioning properly. The hazard does not cause immediate injury.
People using this medical device for therapy may be affected. Those with specific production lots are most at risk.
Check for the product name 'BD SE Burette Set 20 Drops 2 Injection Ports Vented/NonVented' with the reference number 72103E-0006. Affected lots are listed in the recall notice.
Identify the lot number from the product's packaging to see if it matches the affected lots listed in the recall.
The official notice does not specify a remedy.
Affected lots include 20025345, 20025483, 20037040, 20037041, 20037042, 20086605, 20086606, 20086696, 20095927, 20096020, 20105323, 20125599, 20125695, 20125709, 20125710, 21015395.
The recall states flow issues may delay therapy 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-2465-2021 — CAREFUSION CAREFUSION Hello, I own a CAREFUSION that is covered by recall Z-2465-2021 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.
