FDA
Food and Drug Administration · Recall Z-2724-2026 · Jun 10, 2026ICU Medical Plum Solo Precision IV Pump, v1.0.3, Item Number 400010401; infusion pump
ICU Medical, Inc.
The hazard
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. FDA Class II recall.
The remedy
Follow FDA guidance
About this recall
ICU Medical Plum Solo Precision IV Pump, v1.0.3, Item Number 400010401; infusion pump
Affected identifiers
Check these against the label on your unit. An identifier match is how a recall is confirmed, not just suspected.
Model UDI/DI +M335400011Model Serial Numbers: 60000316Model 60000363Model 60000375Model 60000388Model 60000428Model 60000451Model 60000469Model 60000495Model 60000529Model 60000569Model 60000580Model 60000637Model 60000643Model 60000647Model 60000652Model 60000668Model 60000670Model 60000689Model 60000692Model 60000695Model 60000703Model 60000706Model 60000710Model 60000712Would you have heard about this one?
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Start monitoring freeSourced from the Food and Drug Administration’s public recall data. Always verify serial and date ranges against the official notice before acting.