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.
- 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.