FDAMarch 21, 2019device

Prometra Clinician Programmer (Touchscreen) Software version 2.00.29, Cat. No. 12828, used with Prometra and Prometra II Programmable Pumps. For intrathecal infusion.

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

The hazard

The pump shuts down unexpectedly if Error 115, an alarm associated with a watchdog timer timeout, is triggered. There has been an increase of Error 115 occurrences due to a software defect caused by a Healthcare Provider using a Clinician Programmer, Software Version 2.00.29, to program a Bridge or Demand bolus while the pump is set to either a Periodic Flow or Multiple Rates flow mode.

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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