FDAJune 4, 2025device

ADVIA¿ 120/2120/2120i 3-in-1 TESTpoint Control (Norm Control)

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

The hazard

Products have the incorrect platelet (PLT) value assignments for the ADVIA 120/2120/2120i Hematology Systems.

What to do

FDA enforcement status: Ongoing

Brands named

siemens healthcare diagnosticssiemenssiemens healthcare

UPCs

00630414473390

Recall history

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

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