FDAOctober 30, 2017device

Plum 360 Infusion System, List number 30010.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

(1) Under certain conditions, if a malfunction alarm occurs while the pump is in the "Paused" state waiting for the distal pressure to decrease, the pump cannot be turned off and delivery cannot be restarted until the battery is discharged or is disconnected; and (2) when the user accesses the Preventive Maintenance Screen in Service/Biomed Mode with a Total Delivery Time >1,500 hours, the user will not be able to interact with the device and the device must be power cycled.

What to do

FDA enforcement status: Terminated

Brands named

icu medicalicu

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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Plum 360 Infusion System, List number 30010. — Recall Details · AllClear