FDAMarch 22, 2023device

STA Compact Max fully automatic clinical analyzer, Reference Numbers 58602 and 58612

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

The hazard

An internal investigation identified a bug in this firmware version, resulting in the following:Intermittent shortened coagulation times and an increased frequency of occurrence of a technical error reported by the analyzer (error 13).

What to do

FDA enforcement status: Ongoing

Brands named

diagnostica stagodiagnostica

UPCs

036074505898

Recall history

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

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