CareFusion recalls Alaris PCA Module Model 8120 software versions 12.1.0 and older due to potential infusion errors. Affected users should check their software version and contact CareFusion for updates.
1)Error 255-XX-XXX results in inability to edit settings 2)Delay options programming may result in no KVO rate/therapy interruption 3)Software errors results in no low battery alarm/infusion stopping 4)Medium priority KVO/End of Infusion alarms may result in unrecognized infusion completion 5)Custom concentration data entry errors results in concentrations being lower/higher than medication orders
CareFusion is recalling Alaris PCA Module Model 8120 with software versions 12.1.0 and older. These versions may cause infusion errors like incorrect medication doses or therapy interruptions, which could affect patient safety.
The software errors can cause the device to fail to properly edit settings, stop therapy, or alert users about low battery. This may lead to incorrect medication doses or interruptions in pain management treatment.
Patients using the CareFusion Alaris PCA Module Model 8120 with software versions 12.1.0 or older are most at risk. Healthcare providers who administer pain management using this device should also check their software versions.
Check your CareFusion Alaris PCA Module Model 8120 for software versions 12.1.0 or older. The device was sold with these software versions starting from when CareFusion released them.
Look for the software version on your CareFusion Alaris PCA Module Model 8120. Versions 12.1.0 and older are affected.
Reach out to CareFusion for guidance on updating your software to a safe version.
Software versions 12.1.0 and older (including 9.33) are affected.
Check your CareFusion Alaris PCA Module Model 8120 for software versions 12.1.0 or older.
No, but you should check your software version and contact CareFusion for updates to avoid potential issues.
We’ve drafted a message you can send CareFusion to request your refund or repair — edit it as you like.
Subject: Recall Z-1362-2020 — CareFusion CareFusion Hello, I own a CareFusion that is covered by recall Z-1362-2020 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.
