Flowonix Medical Inc recalls

13 recalls on record · latest: May 26, 2021

Official U.S. recall history for Flowonix Medical Inc, compiled from official government records.

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Flowonix Medical Inc recalls Physician Order Form (PL-15400-00, Nov. 2018) distributed to end user used with the following: Prometra Programmable In…

May 26, 2021 · Medical device recalls Moderate risk Physician Order Form (PL-15400-00 Nov 2018) distributed is discontinued due to…

Flowonix Medical Inc recalls Prometra II 20mL Pump. Catalog No. 13827 The device is an implantable infusion pump. GTIN-14 00810335020228

December 24, 2019 · Medical device recalls Moderate risk A pump alarm function anomaly in the pump firmware code may result in the pump…

Flowonix Medical Inc recalls Prometra Programmable 20mL Pump. Catalog No. 91827 The device is an implantable infusion pump. GTIN-14 00810335020XXX (…

December 24, 2019 · Medical device recalls Moderate risk A pump alarm function anomaly in the pump firmware code may result in the pump…

Flowonix Medical Inc recalls US Clinical 20mL Programmable Pump. Catalog No. 01827 The device is an implantable infusion pump. GTIN-14 00810335020082

December 24, 2019 · Medical device recalls Moderate risk A pump alarm function anomaly in the pump firmware code may result in the pump…

Flowonix Medical Inc recalls Prometra Programmable 20mL Pump. Catalog No. 11827 The device is an implantable infusion pump. GTIN-14 00810335020082

December 24, 2019 · Medical device recalls Moderate risk A pump alarm function anomaly in the pump firmware code may result in the pump…

Flowonix Medical Inc recalls Prometra II Programmable 20mL Pump. Catalog No. 93827 The device is an implantable infusion pump. GTIN-14 00810335020YY…

December 24, 2019 · Medical device recalls Moderate risk A pump alarm function anomaly in the pump firmware code may result in the pump…

Flowonix Medical Inc recalls Prometra II 40mL Pump. Catalog No. 16827 The device is an implantable infusion pump. GTIN-14 00810335020242

December 24, 2019 · Medical device recalls Moderate risk A pump alarm function anomaly in the pump firmware code may result in the pump…

Flowonix Medical Inc recalls Prometra Programmable Pump, Cat. No. 11827 For intrathecal infusion.

March 21, 2019 · Medical device recalls Moderate risk The pump shuts down unexpectedly if Error 115, an alarm associated with a watch…

Flowonix Medical Inc recalls Prometra Clinician Programmer (Touchscreen) Software version 2.00.29, Cat. No. 12828, used with Prometra and Prometra I…

March 21, 2019 · Medical device recalls Moderate risk The pump shuts down unexpectedly if Error 115, an alarm associated with a watch…

Flowonix Medical Inc recalls Prometra Programmer (Grand Prime) Software version 2.00.29, Cat. No. 13828, used with Prometra and Prometra II Programm…

March 21, 2019 · Medical device recalls Moderate risk The pump shuts down unexpectedly if Error 115, an alarm associated with a watch…

Flowonix Medical Inc recalls Prometra II Programmable Pump, Cat. No. 13827 For intrathecal infusion.

March 21, 2019 · Medical device recalls Moderate risk The pump shuts down unexpectedly if Error 115, an alarm associated with a watch…

Flowonix Medical Inc recalls Prometra II Programmable Pump (Clinical), Cat. No. 01827 For intrathecal infusion.

March 21, 2019 · Medical device recalls Moderate risk The pump shuts down unexpectedly if Error 115, an alarm associated with a watch…

Flowonix Medical, Inc. recalls PROMETRA II Programmable Infusion Pump, Implantable Infusion Pump, Catalog Number/REF 13827, Part Number PL-31790-02. M…

May 22, 2017 · Medical device recalls Moderate risk Flowonix Medical received a report of a patient implanted with the Prometra II…