CAREFUSION recalls BD Alaris Pump Infusion Burette Sets with potential flow issues that could delay therapy. Affected units include specific lot numbers from 20077170 to 20077320.
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 BD Alaris Pump Infusion Burette Sets that may cause flow problems, leading to therapy delays. This affects patients using insulin pumps or similar medical devices.
The tubing may have issues with flushing or flow, causing partial or complete blockages. This could delay medical treatment but does not typically cause serious injury in normal use.
Patients using the recalled BD Alaris Pump Infusion Burette Sets for insulin or other medical therapies are most at risk. The recall targets specific lot numbers produced in 2007.
Check for the lot numbers 20077170, 20077171, 20077319, or 20077320 on the product packaging. The product is a BD Alaris Pump Infusion Burette Set with SmartSite Y-Sites.
Look for lot numbers 20077170, 20077171, 20077319, or 20077320 on the packaging.
No, the recall does not require immediate discontinuation. The product can be used if it has been safely connected to the female luer of a connecting device.
The official notice does not specify a remedy for this recall. Check with your healthcare provider for guidance.
Check the lot numbers on the packaging: 20077170, 20077171, 20077319, or 20077320.
We’ve drafted a message you can send CAREFUSION to request your refund or repair — edit it as you like.
Subject: Recall Z-2466-2021 — CAREFUSION CAREFUSION Hello, I own a CAREFUSION that is covered by recall Z-2466-2021 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.
