Recall
FDAHealthApril 29, 2026

ICU Medical, Inc. — Plum Duo Precision IV Pump, 40002-0403

⚠️ 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 Precision IV Pump, 40002-0403
Lot code
UDI-DI M335400031 Plum Duo Precision IV Pump v1.2.3

Additional details

UDI-DI M335400031 Plum Duo Precision IV Pump v1.2.3

What should I do?

Recommended action

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

View original FDA notice →

Get Health recall alerts

Delivered to your inbox. Free. No account required.