FDAMay 22, 2017device

PROMETRA II Programmable Infusion Pump, Implantable Infusion Pump, Catalog Number/REF 13827, Part Number PL-31790-02. Manufactured by: Flowonix Medical Inc., --- The correction involves the labeling of the device plus the following Prometra II pump labeling is also being revised: Intrathecal Cath...

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

The hazard

Flowonix Medical received a report of a patient implanted with the Prometra II Programmable Pump who may have received a fatal drug overdose during an MRI procedure. The Prometra II pump has an FDA-approved design feature intended to permit safe exposure to an MRI without removing drug from the reservoir.

What to do

FDA enforcement status: Terminated

Brands named

flowonix medicalflowonix

Recall history

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

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