PlainRecalls
FDA Devices Critical Class I Ongoing

Plum Duo Infusion System, List Number: 400020401

Reported: August 13, 2025 Initiated: July 11, 2025 #Z-2129-2025

Product Description

Plum Duo Infusion System, List Number: 400020401

Reason for Recall

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

Details

Recalling Firm
ICU Medical, Inc.
Units Affected
4677 units
Distribution
US Nationwide.
Location
Lake Forest, IL

Frequently Asked Questions

What product was recalled?
Plum Duo Infusion System, List Number: 400020401. Recalled by ICU Medical, Inc.. Units affected: 4677 units.
Why was this product recalled?
ICU Medical identified two sequences of programming events and alarm interactions that may cause the user interface to become unresponsive.
Which agency issued this recall?
This recall was issued by the FDA Devices on August 13, 2025. Severity: Critical. Recall number: Z-2129-2025.