Recall
FDAHealthApril 29, 2026

ICU Medical, Inc. — Plum Duo Infusion Pump, 40002-0401

⚠️ 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.

Is this relevant to me?

Geography
Nationwide
Source agency
FDA
Category
Health
Published
April 29, 2026

Worldwide - US Nationwide distribution in the states of ID, IL, IN, KS, MA, MD, NM, NY, PA, TN, TX and the country of Canada.

What's affected?

Product
Plum Duo Infusion Pump, 40002-0401
Lot code
UDI-DI M335400021 Plum Duo Infusion Pump v1.2.3

Additional details

UDI-DI M335400021 Plum Duo Infusion Pump v1.2.3

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated Quantity affected: 13,613.

View original FDA notice →

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