FDAJune 30, 2020device

Alaris Syringe Module Model 8110 - Product Usage: is intended to provide trained healthcare caregivers a way to automate the programming of infusion parameters, thereby decreasing the amount of manual steps necessary to enter infusion data.

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

The hazard

LED display, which provides infusion or patient monitoring values, on the module may have segments that appear dim.

What to do

FDA enforcement status: Ongoing

Brands named

carefusion 303carefusion

Recall history

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

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