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Hologic, Inc recalls BioZorb Marker. Radiographic soft tissue marker.
Recalled December 4, 2024 · FDA recall Z-0328-2025 · Hologic
Hazard
Firm received reports of adverse events/complications that include serious injuries, such as pain, infection, rash, device migration, device erosion, seroma, and discomfort. · FDA Class I
Units
12,710 units
Sold at
Domestic: US Nationwide Distribution.
Description
Firm received reports of adverse events/complications that include serious injuries, such as pain, infection, rash, device migration, device erosion, seroma, and discomfort.
Product
BioZorb Marker. Radiographic soft tissue marker.
Manufacturer(s)
Hologic, Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →