medical Class II Updated 2020-02-19

Flowonix Medical Inc recalls Prometra Programmable 20mL Pump. Catalog No. 91827 The devic

Recalled Product

Prometra Programmable 20mL Pump. Catalog No. 91827 The device is an implantable infusion pump. GTIN-14 00810335020XXX (XXX = in-country language specific)

Hazard / Issue

A pump alarm function anomaly in the pump firmware code may result in the pump not sending the expected error code notifications to the Programmer, or not emit an audible alarm tone in certain "out of tolerance" conditions associated with the pump's valve system.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: All units with pump firmware version 0.26 manufactured from 2012 until the present time.
View official government recall

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