FDAAugust 15, 2024device

Alaris System PC Unit Model 8015 - 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

10885403516023108854035152311088540380154910885403801532108854038015181088540351928410885403519215

Recall history

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

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