FDAJanuary 15, 2025device

Brand Name: Sertera Biopsy Device Product Name: Sertera Biopsy Device Model/Catalog Number: Sertera-14 Software Version: N/A Product Description: Instrument, Biopsy Component: N/A

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

The hazard

Devices presented a condition in which the inner needle separated from the hub and produced a longer throw of the inner needle or dislodgement.

What to do

FDA enforcement status: Ongoing

Brands named

hologic

UPCs

15420045504066

Recall history

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

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