FDAJune 15, 2017device

Plum 360 Infusion System

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

The hazard

Potential for the Connectivity Engine Module of the affected unit to disengage from the main chassis, causing the unit to shut down without an alarm notification. This would delay initiation of therapy or interrupt an infusion.

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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