FDAApril 17, 2014device

The Patient Control Module (PCM) is used in conjunction with a Baxter infusor as a single use device for the control of intermittent bolus doses of medication based on patient demand.

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

The hazard

Potential for device malfunction resulting in flow when the device should not be flowing

What to do

FDA enforcement status: Terminated

Brands named

baxter healthcarebaxter

Recall history

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

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