FDAOctober 9, 2020device

Ultra2 Resolution Variants System for Abnormal Hemoglobin Quantitation

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

The hazard

The product did not receive pre-market approval or clearance.

What to do

FDA enforcement status: Terminated

Brands named

primus

Recall history

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

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