Recall Z-2723-2026— ICU Medical, Inc.

Name: FDA recall Z-2723-2026
Creator: U.S. Food and Drug Administration
Published: 2026-06-10

Class II · Ongoing

Class II FDA medical device recall by ICU Medical, Inc., initiated 2026-06-10. Product: ICU Medical Plum Duo Infusion Pump, v1.2.3: 1) Item Number 400020401 and 2) Item Number 400020403; infusion pump. Reason: In a specific scenario, the pump will not decrement the Volume to be Infused (VTBI) displayed on the Delivery screen and may deliver up to twice the VTBI at the programmed rate..

Recalling firm: ICU Medical, Inc.
Classification: Class II
Status: Ongoing
Initiated: 2026-06-10
Firm location: Lake Forest, IL, United States

Product description

ICU Medical Plum Duo Infusion Pump, v1.2.3: 1) Item Number 400020401 and 2) Item Number 400020403; infusion pump

Reason for recall

In a specific scenario, the pump will not decrement the Volume to be Infused (VTBI) displayed on the Delivery screen and may deliver up to twice the VTBI at the programmed rate.

Data sourced from openFDA. This site is unofficial and independent of the FDA.