FDAMarch 21, 2019device

Prometra II Programmable Pump (Clinical), Cat. No. 01827 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. Error 115 can also occur if dendrites form or if the pump is dropped.

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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Prometra II Programmable Pump (Clinical), Cat. No. 01827 For intrathecal infusion. — Recall Details · AllClear