FDAMay 16, 2019device

GE Pristina Serena - Product Usage: Pristina Serena is an optional accessory of Senographe Pristina intended to provide accurate location of lesions in the breast in three dimensions.

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

The hazard

Potential slippage of the biopsy positioner when the gantry is rotated during a biopsy procedure.

What to do

FDA enforcement status: Terminated

Brands named

ge healthcare

Recall history

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

Own something like this?

AllClear screens your whole list against every CPSC, FDA, USDA and NHTSA recall — and tells you the day a new one names something you own.

Start free — 200 items, no card →