The U.S. Food and Drug Administration has sent a warning letter to Marlborough, Mass.-based medical technology company ...

FDA issues warning to Hologic, citing manufacturing and safety violations for BioZorb devices. Patient safety risks and reporting failures highlighted ...

Hologic stopped manufacturing the device after reports of serious adverse events in patients who had the markers implanted in breast tissue.

Hologic Inc. has received a warning letter from the Food and Drug Administration regarding its BioZorb product line, even ...

Trichomoniasis companies are Sekisui Diagnostics, Becton Dickinson and Company, Hologic, Pfizer ... disease and increasing number of drug launches and approvals are some of the important factors ...

Leading members of the Democratic Women’s Caucus asked the FDA to address concerns about tampon safety after seeing the results of a study published in the journal Environment International. The study ...

With the FDA warning that these oysters may have been distributed beyond Washington and Oregon, restaurants and retailers in these states are advised to dispose of or return the product immediately.

The CPSC notified Apple that AirTag was in violation of warning label requirements related to Reese’s Law. Essentially the law requires products with button cell or coin batteries to include ...

I was so confused. He was so healthy." The Food and Drug Administration (FDA) sent a letter on Dec. 16 to veterinarians nationwide advising them about the potential dangers of Librela. That letter ...

A recall of products, including onions, from Gracie's Kitchen has been given a Class II risk classification from the FDA over fears of listeria monocytogenes contamination. The recall impacts ...

California officials, along with dozens of others across the country, received letters this week from Stephen Miller’s nonprofit, America First Legal, warning them of the consequences for ...