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ICU Medical, Inc. recalls Plum Duo Precision IV Pump, 40002-0403
Recalled June 17, 2026 · FDA recall Z-2313-2026 · ICU Medical
Hazard
Under certain conditions, the pump may not display a soft limit alert, and will not notify the clinician of a soft limit violation before confirming and starting delivery. This may potentially lead to under- or over-delivery. · FDA Class II
Units
13,613
Sold at
Worldwide - US Nationwide distribution in the states of ID, IL, IN, KS, MA, MD, NM, NY, PA, TN, TX and the country of Canada.
Description
Under certain conditions, the pump may not display a soft limit alert, and will not notify the clinician of a soft limit violation before confirming and starting delivery. This may potentially lead to under- or over-delivery.
Product
Plum Duo Precision IV Pump, 40002-0403
Manufacturer(s)
ICU Medical, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →