FDAMarch 3, 2022device

Atellica IM Enhanced Estradiol (eE2) 100T - In vitro diagnostic use in the quantitative determination of estradiol SMN: 10995561 All lots

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

The hazard

Falsely Elevated Results Observed with Plasma Specimens, could lead a clinician to misinterpret patient results

What to do

FDA enforcement status: Ongoing

Brands named

siemens healthcare diagnosticssiemenssiemens healthcare

UPCs

00630414598857

Recall history

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

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