CareFusion recalls Alaris Pump Module 8100 devices with dim LED displays that could lead to inaccurate infusion monitoring readings. 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 Pump Module 8100 devices because their LED displays may appear dim, potentially causing inaccurate infusion monitoring readings. This could affect healthcare caregivers using the device for automated infusion programming.
The LED display segments may appear dim, which could lead to inaccurate readings of infusion or patient monitoring values. This might cause healthcare providers to misinterpret the device's status, though the risk is not severe.
Healthcare caregivers using the Alaris Pump Module 8100 for automated infusion programming are most likely affected. The recall applies to all units with specific serial numbers.
Check the serial number on the Alaris Pump Module 8100 device. The recall applies to all units with specific serial numbers as described in the official notice.
Identify the serial number on your Alaris Pump Module 8100 device to confirm if it is affected.
The LED display segments may appear dim, which could lead to inaccurate infusion monitoring readings.
Check the serial number on your Alaris Pump Module 8100 device to see if it is affected. The recall applies to all units with specific serial numbers.
The recall does not mention a fix or remedy; affected units require checking the serial number.
We’ve drafted a message you can send CareFusion to request your refund or repair — edit it as you like.
Subject: Recall Z-2822-2020 — CareFusion CareFusion Hello, I own a CareFusion that is covered by recall Z-2822-2020 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.
