The FDA is recalling more than 7,000 bottles of the antidepressant duloxetine due to a possible cancer-causing chemical.

That's why it's so distressing to learn of a new drug recall issued by the U.S. Food and Drug Administration (FDA) in which 7 ...

A pharmaceutical company issued a recall this month for thousands of bottles of duloxetine, a medicine often prescribed to ...

The FDA recently announced a recall of over 7,000 bottles of duloxetine after detecting elevated levels of ...

A pharmaceutical company issued a recall this month for thousands of bottles of duloxetine, a medicine often prescribed to ...

We are fully cooperating with the FDA on their investigation and have taken immediate action by removing all affected products related to this recall from our shelves," Marisa Kutansky ...

In an update regarding the ongoing recall of pre-packaged muffins, the U.S. Food and Drug Administration (FDA) has classified the recall as Class II, due to the presence of undeclared allergens.

Thermo Fisher's Greenville, N.C. plant has been found in breach of US FDA regulations, including twice this year FDA's most recent inspection of Thermo Fisher plant found shortfalls in ...

On Friday, the FDA approved Exact Sciences Corp.’s (NASDAQ:EXAS) Cologuard Plus test, the company’s next-generation multi-target stool DNA test. The Cologuard Plus test is now approved for ...

TOPEKA (KSNT) – A Colorado-based candy shop issued a recall after discovering one of its products caused an allergic reaction. The Food and Drug Administration (FDA) said Hammond’s Candies is ...

The U.S. Food and Drug Administration (FDA) has issued an update to its ongoing recall of a sriracha hot sauce product, which is now classified as a Class II recall. Class II classifications are ...

DSM-Firmenich says the FDA is expected to decide within the next 17.5 months — by March 2026 — on the company's request to approve the sunscreen ingredient bemotrizinol, branded as PARSOL Shield.