ICU Medical, Inc.: Device Recall
Recall #Z-1120-2026 · 12/15/2025
Class II: Risk
Recall Details
- Recall Number
- Z-1120-2026
- 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 Solo Precision IV Pump, List Numbers: 400010401 (US), 400011001 (Philippines)
Distribution Pattern
Worldwide distribution - US Nationwide and the country of Philippines.
Other Recalls by ICU Medical, Inc.
- Class II: Risk 12/19/2025
- Class II: Risk 12/19/2025
- Class II: Risk 12/19/2025
- Class II: Risk 12/15/2025
- Class II: Risk 12/15/2025
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.