FDAJanuary 23, 2017device

Merge LIS

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

The hazard

A defect in the software resulted in medications that are not associated with the patient (i.e., medications that the patient is not currently taking) appearing on their report.

What to do

FDA enforcement status: Terminated

Brands named

merge healthcaremerge

Recall history

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

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