FDADecember 24, 2019device

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

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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.

What to do

FDA enforcement status: Ongoing

Brands named

flowonix medicalflowonix

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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