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Flowonix Medical Inc: Medical Device Recalls in 2019

Updated on March 25, 2026.

According to to data from the FDA, there were 5 medical device recalls made by Flowonix Medical Inc in 2019. See the details of the recalls below.

You can see similar recalls for other firms.

Data Source: FDA.
See this for other years:
2017
2019
2020
2021
  • Prometra II Programmable Pump (Clinical), Cat. No. 01827 For intrathecal infusion.
  • Prometra Clinician Programmer (Touchscreen) Software version 2.00.29, Cat. No. 12828, used with Prometra and Prometra II Programmable Pumps. For intrathecal infusion.
  • Prometra II Programmable Pump, Cat. No. 13827 For intrathecal infusion.
  • Prometra Programmer (Grand Prime) Software version 2.00.29, Cat. No. 13828, used with Prometra and Prometra II Programmable Pumps. For intrathecal infusion.
  • Prometra Programmable Pump, Cat. No. 11827 For intrathecal infusion.
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