FDAOctober 4, 2019device

Prismaflex Control Unit, software versions below 7.21

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

The hazard

Communication error alarms may result in interruption of therapy, delay in therapy, or blood loss due to non-restitution of blood in the extracorporeal circuit.

What to do

FDA enforcement status: Ongoing

Brands named

baxter healthcarebaxter

UPCs

07332414105266

Recall history

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

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