Class II

Medical Device Recall: ICU Medical Plum Solo Precision IV Pump, v1.0.3, Item Number 400010401; infusion pump

ICU Medical, Inc. · June 10, 2026

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.

Distribution

Worldwide distribution - US Nationwide and the country of Canada.

States Affected

NATIONWIDE

Quantity Affected

5059 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2724-2026

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.