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The U.S. Food and Drug Administration (FDA) has issued a recall of the Hologic, Inc. BioZorb marker due to complications with implanted devices. The agency identified this as a Class I recall, the most serious type of recall. Details issued in a written notice by the FDA on May 22 and are shared here.
The U.S. Food and Drug Administration on Wednesday classified a recall of Hologic's devices that are implanted in soft tissue such as breast tissue as "most serious", and...
Health news and commentary gathered by <em>MedPage Today</em> staff
Medical technology company Hologic warns customers of potential risks linked to implantable device used for procedures. FDA reports 71 injuries.
The U.S. Food and Drug Administration on Wednesday classified a recall of Hologic's devices that are implanted in soft tissue such as breast tissue as most serious, and urged doctors to more actively...