> ## Content Index
> Fetch the complete content index at: https://www.fdaweb.com/llms.txt
> Use this file to discover other available public pages before exploring further.

# ICU Medical Expands Class 1 Recall of Infusion Pumps
- URL: https://www.fdaweb.com/icu-medical-expands-class-1-recall-of-infusion-pumps/
- Published: 2024-08-20T12:00:00.000Z
- Updated: 2026-09-14T14:38:53.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5157617

ICU Medical is expanding a Class 1 recall of its Plum 360, Plum A+ and Plum A+3 Infusion Systems to update the use instructions due to a manufacturing defect with the batteries, which can result in diminished battery life. The updated notice expands affected products from [a 3/2023 notice](https://www.fda.gov/medical-devices/medical-device-recalls/icu-medical-recalls-replacement-batteries-plum-360-plum-and-plum-a3-infusion-systems-due-diminished?ref=fdaweb.com) and now includes all replacement batteries manufactured by CSB.

“The use of affected products may cause serious injury or death to patients due to interruption, under-infusion, or delays in the delivery of critical fluids, blood products, and medications,” the [recall notice](https://www.fda.gov/medical-devices/medical-device-recalls/infusion-pump-battery-correction-icu-medical-updates-instructions-use-regarding-batteries-plum-360?utm%5Fmedium=email&utm%5Fsource=govdelivery) says. The batteries are used when the pump is not plugged into AC power, such as when a patient is being transported.

The large-volume infusion pumps are used to give fluids to patients in precisely controlled infusion amounts and rates.