FDASeptember 21, 2023device

8713051U, Infusomat Large Volume Pump, Wireless; Volumetric Infusion Pump System

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

The hazard

Upstream occlusion alarm may sound when no occlusion exists, and the device will stop pumping. Interruption to the infusion of high-risk medications may lead to hemodynamic instability requiring medical intervention to prevent permanent impairment to body structures or body functions. In some cases, this may be life-threatening or may lead to death.

What to do

FDA enforcement status: Ongoing

Brands named

b braun medical

UPCs

04046964660887

Recall history

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

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