FDAMay 17, 2021device

CytoCell DiGeorge/VCFS TUPLE1 Region and 22q13.3 Region Probe, Model Number LPU004-A. analyte specific reagent for in vitro diagnostics

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

The hazard

The device may show unexpected locus specific signals in addition to those at 22q. Users may observe faint additional locus specific signals at 20p12/13.

What to do

FDA enforcement status: Terminated

Brands named

cytocell

Recall history

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

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