FDAJune 12, 2017device

Alaris Pump Module model 8100

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

The hazard

There is a potential risk that could cause unintended flow in the older, centered sear door latch design in the Alaris Pump module model 8100.

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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