FDAJune 30, 2020device

Alaris System PC Unit Model 8015. modular infusion pump and monitoring system

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

The hazard

If one or more screws or washers are loose or missing causing the battery not to be properly secured to the PC Unit, that is running on battery power, the system may experience a power loss with a prolonged, non-silenceable alarm. Power loss may result in an interruption of patient therapy or monitoring.

What to do

FDA enforcement status: Terminated

Brands named

carefusion 303carefusion

Recall history

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

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