Icu Medical, Inc.
951 CALLE AMANECER, SAN CLEMENTE, CA, US
Registered product codes
92 product codes
Recent MDR events
15,840 on file
- CADD Solis HPCA PumpJul 31, 2026Malfunction3012307300-2026-07767
- CADD Legacy Plus PumpJul 31, 2026Malfunction3012307300-2026-07769
- CADD Solis HPCA PumpJul 31, 2026Malfunction3012307300-2026-07770
- CADD Solis HPCA PumpJul 31, 2026Malfunction3012307300-2026-07771
- CADD Solis HPCA PumpJul 31, 2026Malfunction3012307300-2026-07772
- CADD Solis HPCA PumpJul 31, 2026Malfunction3012307300-2026-07773
- CADD Solis HPCA PumpJul 31, 2026Malfunction3012307300-2026-07774
- Jelco Safety ProtectIV Plus CathetersJul 31, 2026Malfunction3012307300-2026-07775
- CADD Solis HPCA PumpJul 31, 2026Malfunction3012307300-2026-07776
- CADD Solis HPCA PumpJul 31, 2026Malfunction3012307300-2026-07778
Recalls
647 on file
- Open, ClassifiedJul 17, 2026
ICU Medical became aware of an increased likelihood of leakage in specific Lots of L-70 HOTLINE Fluid Warming Sets due to potentially inadequate solvent application at the tubing to return connector bond.
View FDA record ↗ - Open, ClassifiedJul 10, 2026
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.
View FDA record ↗ - Open, ClassifiedJul 10, 2026
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.
View FDA record ↗ - Open, ClassifiedJun 5, 2026
Under certain conditions, the pump may not display a soft limit alert, and will not notify the clinician of a soft limit violation before confirming and starting delivery. This may potentially lead to under- or over-delivery.
View FDA record ↗ - Open, ClassifiedJun 5, 2026
Under certain conditions, the pump may not display a soft limit alert, and will not notify the clinician of a soft limit violation before confirming and starting delivery. This may potentially lead to under- or over-delivery.
View FDA record ↗ - Open, ClassifiedJun 5, 2026
Under certain conditions, the pump may not display a soft limit alert, and will not notify the clinician of a soft limit violation before confirming and starting delivery. This may potentially lead to under- or over-delivery.
View FDA record ↗ - Open, ClassifiedMay 18, 2026
Oncology sets/closed system transfer devices with extension sets may leak resulting in therapy delayed if noticed and corrected during setup, but if the leak occurs during therapy this may result in therapy interruption with the potential for the patient to receive less infusion solution than intended. Exposure of hazardous substances to the patient, caregiver, or pharmacy technician is possible.
View FDA record ↗ - Open, ClassifiedJan 16, 2026
Needle free access device intended as accessory to vascular access used in hemodialysis or accessory to intravascular administration sets has a silicone seal which may bulge at the top, separate from the body, tear; may result in fluid leaks, occluded fluid flow, inability to inject/withdraw blood product, delayed/interrupted therapy, exposure to biological contaminants, air infused into the body
View FDA record ↗ - Open, ClassifiedJan 16, 2026
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.
View FDA record ↗ - Open, ClassifiedJan 16, 2026
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.
View FDA record ↗
Compliance history
Matched by FEI 2025816.
FDA inspections
0 on file
No inspections on file for this FEI number.
Inspection citations
0 on file
No citations on file for this FEI number.
Compliance actions
0 on file
No warning letters or injunctions on file for this FEI number.
Import refusals
0 on file
No import refusals on file for this FEI number.