FDASeptember 22, 2020device

Model 3300 LATITUDE Programming System with installed Model 3892 ALTRUA, INSIGNIA I, NEXUS I Software Support Application

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

The hazard

There is potential when a user changes an EGM trace channel with a Manual Pace Threshold test in progress that the newly modified trace channel may change to a flat line.

What to do

FDA enforcement status: Terminated

Brands named

boston scientificboston

Recall history

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

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