FDAMarch 24, 2021device

Aftermarket Alaris Infusion Pump Module Model 8100 Front Bezel, installed by Pacific Medical Group (DBA Avante Health Solutions)

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

The hazard

Aftermarket front bezel components were installed during service/repair, not by the original manufacturer, within infusion pump modules. Over time, the posts on the front bezel component may crack or separate. Separation of one or more bezel posts could lead to free flow, over infusion, under infusion, or interruption of infusion.

What to do

FDA enforcement status: Ongoing

Brands named

pacific medicalpacific

Recall history

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

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