Flowonix Medical recalls
Flowonix Medical appears in 13 official U.S. recall notices indexed by RecallRadar, most recently on 2021-07-07.
Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.
- Physician Order Form (PL-15400-00, Nov. 2018) distributed to end user used with the following: Prometra Programmable Infusion Pump System:…
FDA Device · Class II · 2021-07-07 · Flowonix Medical - US Clinical 20mL Programmable Pump
FDA Device · Class II · 2020-02-19 · Flowonix Medical - Prometra II 40mL Pump
FDA Device · Class II · 2020-02-19 · Flowonix Medical - Prometra II Programmable 20mL Pump
FDA Device · Class II · 2020-02-19 · Flowonix Medical - Prometra Programmable 20mL Pump
FDA Device · Class II · 2020-02-19 · Flowonix Medical - Prometra Programmable 20mL Pump
FDA Device · Class II · 2020-02-19 · Flowonix Medical - Prometra II 20mL Pump
FDA Device · Class II · 2020-02-19 · Flowonix Medical - Prometra II Programmable Pump (Clinical), Cat
FDA Device · Class II · 2019-06-12 · Flowonix Medical - Prometra Programmer (Grand Prime) Software version 2.00.29, Cat
FDA Device · Class II · 2019-06-12 · Flowonix Medical - Prometra II Programmable Pump, Cat
FDA Device · Class II · 2019-06-12 · Flowonix Medical - Prometra Programmable Pump, Cat
FDA Device · Class II · 2019-06-12 · Flowonix Medical - Prometra Clinician Programmer (Touchscreen) Software version 2.00.29, Cat
FDA Device · Class II · 2019-06-12 · Flowonix Medical - PROMETRA II Programmable Infusion Pump, Implantable Infusion Pump, Catalog Number/REF 13827, Part Number PL-31790-02
FDA Device · Class II · 2017-07-26 · Flowonix Medical