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

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

The rate of warnings initiated by the FDA continues to rise in the pharma and medical device industries. Knowing how to best ...

Applied Therapeutics, a clinical-stage biopharmaceutical company, is under heightened scrutiny following the issuance of a November 2024 ...

In a warning letter posted online late last month, the FDA scolded Viatris over a range of production slights at the ...

On the heels of a Food and Drug Administration (FDA) warning letter to the manufacturer of CBD-coated tampons marketed to ...

Fagron (ARSUF) has refocused its M&A strategy, regaining market trust despite recent FDA issues. Read why I think the stock ...

In a regulatory filing on Monday, Integra LifeSciences (IART) said that on December 19, 2024, a subsidiary received a warning letter from the ...

Integra Lifesciences recently received an FDA warning letter pertaining to quality systems issues at several facilities.

As part of its enforcement activities, the Food and Drug Administration sends warning letters to entities under its jurisdiction. Some letters are not ...

After thousands of complaints about complications, the FDA has issued an open letter to veterinarians to be alert to serious ...