CareFusion recalls Alaris Syringe Module Model 8110 with software versions 12.1.0 and older due to potential infusion errors. Affected users should check their device 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 its Alaris Syringe Module Model 8110 with specific software versions because software errors could cause infusion problems like incorrect medication doses or therapy interruptions. This affects users who rely on the device for medical treatments.
Software errors in the device can cause incorrect medication concentrations, therapy interruptions, or failure to alert about low battery. This may lead to improper dosing or stopped treatments if the device doesn't recognize infusion completion.
Users of the CareFusion Alaris Syringe Module Model 8110 with software versions 12.1.0 or older are most at risk. Patients receiving insulin or other medications through this device may experience infusion errors.
Check your device for the model number 8110 and software version 12.1.0 or older. The recall covers devices sold with these specific software versions.
Look for the model number 8110 and software version 12.1.0 or older on your CareFusion Alaris Syringe Module.
Software versions 12.1.0 and older (including 9.33) are affected.
No immediate stop is required; check your device version and contact CareFusion for updates.
Software errors could cause incorrect medication doses, therapy interruptions, or failure to alert about low battery.
We’ve drafted a message you can send CareFusion to request your refund or repair — edit it as you like.
Subject: Recall Z-1361-2020 — CareFusion CareFusion Hello, I own a CareFusion that is covered by recall Z-1361-2020 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.
