FDAAugust 15, 2024device

Alaris Syringe Module Model 8110, 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

108854035160471088540351532310885403811043108854038110361088540381101210885403424267

Recall history

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

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