CareFusion recalls Alaris Extension Sets (Models 20022 and 30914) due to incorrect priming volume from manufacturing defects. Affected units include specific lot numbers. Consumers should contact CareFusion for details.
Reports of incorrect priming volume due to manufacturing with incorrect tubing.
CareFusion is recalling Alaris Extension Sets with microbore tubing models 20022 and 30914 because they may have incorrect priming volumes due to manufacturing defects. This could lead to improper medication or fluid administration during medical procedures.
The extension sets may have incorrect tubing that causes inaccurate priming volumes. This means the amount of fluid or medication delivered to a patient could be less than intended, potentially leading to treatment errors.
Healthcare professionals using these extension sets for intravenous medication administration are most at risk. Patients receiving treatments through these sets may be affected if the sets are used incorrectly.
Check for model numbers 20022 or 30914 on the extension sets. Affected units include specific lot numbers: 16087775, 16127995, 16127518, and 17097167.
Identify the model number on the extension set (20022 or 30914) and compare with the listed lot numbers.
The extension sets may have incorrect tubing that causes inaccurate priming volumes, potentially leading to improper medication or fluid administration.
Lot numbers 16087775, 16127995 for model 20022, and 16127518, 17097167 for model 30914.
The recall does not require immediate discontinuation; however, affected units should be checked and contacted for further instructions.
We’ve drafted a message you can send CareFusion to request your refund or repair — edit it as you like.
Subject: Recall Z-2111-2018 — CareFusion CareFusion Hello, I own a CareFusion that is covered by recall Z-2111-2018 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.
