CareFusion recalls Alaris Syringe Module Model 8110 for potential dim LED display that could lead to inaccurate infusion monitoring. Affected units have specific serial numbers.
LED display, which provides infusion or patient monitoring values, on the module may have segments that appear dim.
CareFusion is recalling Alaris Syringe Module Model 8110 syringes because their LED display may appear dim, potentially causing inaccurate infusion monitoring. This could matter for healthcare workers using the device to program infusion settings.
The LED display on the module may show dim segments, which could lead to inaccurate readings of infusion or patient monitoring values. This might cause healthcare workers to misinterpret the device's status during programming.
Healthcare caregivers using the Alaris Syringe Module Model 8110 for infusion programming are most at risk. The recall affects specific serial numbers of the device.
Check the serial number on the Alaris Syringe Module Model 8110. The product is intended for trained healthcare caregivers to automate infusion programming.
Identify the serial number on the Alaris Syringe Module Model 8110 to confirm if it is affected.
The LED display on the module may appear dim, which could lead to inaccurate infusion monitoring readings.
Check the serial number on the Alaris Syringe Module Model 8110, as the product is intended for trained healthcare caregivers to automate infusion programming.
The recall does not specify a remedy, so contact CareFusion directly for guidance.
We’ve drafted a message you can send CareFusion to request your refund or repair — edit it as you like.
Subject: Recall Z-2823-2020 — CareFusion CareFusion Hello, I own a CareFusion that is covered by recall Z-2823-2020 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
