Class I

Medical Device Recall: Plum Duo Infusion System, List Number: 400020401

ICU Medical, Inc. · July 11, 2025

Reason for Recall

ICU Medical identified two sequences of programming events and alarm interactions that may cause the user interface to become unresponsive.

Distribution

US Nationwide.

States Affected

NATIONWIDE

Quantity Affected

4677 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2129-2025

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.