FDAMarch 26, 2021device

Alaris Pump Module, Model 8100, serviced/repaired by Infusion Pump Repair with an impacted bezel repair part

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

The hazard

Bezel repair parts used, not by the original manufacturer, to service and repair infusion pump modules, may over time experience cracking or separation of the posts from the bezel. The separation of one or more bezel repair part posts may result in free flow, over infusion, under infusion or interruption of infusion.

What to do

FDA enforcement status: Ongoing

Brands named

infusion pump repairinfusioninfusion pump

Recall history

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

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Alaris Pump Module, Model 8100, serviced/repaired by Infusion Pump Repair with an impacted bezel repair part — Recall Details · AllClear