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Hologic, Inc recalls Sertera Biopsy Device, Sterile; Used primarily in ultrasound-guided breast biopsies.
Recalled September 28, 2016 · FDA recall Z-2869-2016 · Hologic
Hazard
Incorrect label on the Sertera Biopsy Kit · FDA Class II
Units
570 units
Sold at
Nationwide.
Description
Incorrect label on the Sertera Biopsy Kit
Product
Sertera Biopsy Device, Sterile; Used primarily in ultrasound-guided breast biopsies.
Manufacturer(s)
Hologic, Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →