FDAOctober 24, 2025device

Senographe Pristina, Pristina Serena, and Pristina Serena 3D. for screening and diagnostic mammography

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

The hazard

Some Senographe Pristina systems either have a missing or an incorrect X-Ray Warning label, which is a nonconformance to FDA Regulation 21 CFR ¿1020.30(j).

What to do

FDA enforcement status: Ongoing

Brands named

ge medical systems

UPCs

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Recall history

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

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