CareFusion recalls Alaris Syringe Module Model 8110 infusion pumps due to cleaning risks causing infusion interruptions. Users must follow updated cleaning instructions to prevent therapy interruptions.
Cleaning agents may damage Inter-Unit Interface (IUI) Connectors, which may lead to interruption of communication or power between PC Unit and modules, which may result in an infusion that stops with a CHANNEL DISCONNECTED message, and an audio/visual alarm on the PC Unit and an interruption of therapy or monitoring.
CareFusion recalls Alaris Syringe Module Model 8110 infusion pumps because improper cleaning can damage internal connectors, causing infusion stops and alarms. This affects patients using these pumps for therapy monitoring.
Cleaning agents can damage the Inter-Unit Interface connectors, which are critical for communication between the pump and modules. If damaged, the system may stop therapy or monitoring with a 'CHANNEL DISCONNECTED' message and alarms.
Patients using CareFusion Alaris Syringe Module Model 8110 infusion pumps are most at risk. Healthcare providers who handle these devices during cleaning may also be affected.
Check for the Alaris Syringe Module Model 8110 label on the pump. This model is used in modular infusion pumps for therapy monitoring systems.
Use the manufacturer's updated cleaning instructions and IUI covers for all serial numbers to prevent connector damage.
Cleaning agents may damage the Inter-Unit Interface connectors, causing infusion interruptions and therapy stops.
Follow the updated cleaning instructions and use IUI covers to prevent connector damage.
The recall describes potential infusion stops and alarms, 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-2719-2020 — CareFusion CareFusion Hello, I own a CareFusion that is covered by recall Z-2719-2020 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.
