ICU Medical, Inc.: Device Recall

Recall #Z-1118-2026 · 12/15/2025

Class II: Risk

Recall Details

Recall Number
Z-1118-2026
Classification
Class II
Product Type
Device
Recalling Firm
ICU Medical, Inc.
Status
Ongoing
Date Initiated
12/15/2025
Location
Lake Forest, IL, United States
Voluntary/Mandated
Voluntary: Firm initiated

Reason for Recall

Plum Solo and Duo Infusion pumps include a feature, that when selected, automatically flushes the downstream line after a piggyback therapy. The programmed flush volume is delivered from the primary line container at the piggyback therapy rate after the piggyback therapy is complete. In certain cases, as described below, the clinician may receive an Upper Hard Limit (UHL) or Lower Hard Limit (LHL) Violation message when programming a piggyback flush, which prevents the flush from being programmed.

Product Description

ICU Medical Plum Duo Infusion Pump, List Numbers: 400020401 (US), 400021001 (Philippines)

Distribution Pattern

Worldwide distribution - US Nationwide and the country of Philippines.

Other Recalls by ICU Medical, Inc.

View all recalls by ICU Medical, Inc. →

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.