FDASeptember 23, 2019device

Atellica CH 930 Analyzer

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

The hazard

Potential for calibration error resulting in QC failures after the calibration run with QC and patient results being 5 times higher.

What to do

FDA enforcement status: Terminated

Brands named

siemens healthcare diagnosticssiemenssiemens healthcare

UPCs

00630414002163

Recall history

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

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Atellica CH 930 Analyzer — Recall Details · AllClear