FDAAugust 15, 2024device

Alaris EtCO2 Module Model 8300, 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

1088540383002010885403830013

Recall history

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

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