FDAAugust 15, 2024device

Alaris PCA Module Model 8120, a modular infusion pump and monitoring system

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

The hazard

Due to affected devices that may have bent female IUI connector and may not be operable and potentially cause delays in the start of the infusion or monitoring.

What to do

FDA enforcement status: Ongoing

Brands named

carefusion 303carefusion

UPCs

108854035160301088540351531610885403812033108854038120261088540349429110885403812002

Recall history

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

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