The FDA in 2022 had banned Juul's four varieties of tobacco and menthol-flavored pods and the e-cigarette device after it ...

Prestige Consumer Healthcare Inc. issued a voluntary recall for more than 10,000 cases of honey cough syrup on June 17.

Health Secretary Robert F. Kennedy Jr. has repeatedly said that he wants to fix the way the government provides care to ...

The FDA accepted Aldeyra's resubmitted NDA for reproxalap after previous rejections due to efficacy concerns, despite no ...

Targeted Oncology connects oncology professionals with updates on immunotherapy, biomarkers, cancer pathways, and targeted ...

Due to concerns surrounding its effectiveness, the US Food and Drug Administration (FDA) ended the Rare Pediatric Disease Designation (RPDD) programme in late 2024.

As such, the FDA has classified the New Mexico Pinon Coffee pod recall as a Class III risk. The FDA defines such a risk as “a ...

More than 67,000 cases of deodorant, sold at Walmart and other retailers across the country, were recalled last week due to ...

The move is expected to cause a “near-term stock out of Bicillin L-A,” Pfizer said in its statement, with the drugmaker now ...

The regulator allowed the company’s original vaporizer and refill cartridges in tobacco and menthol flavors to remain on the U.S. market.

A.P. Deauville recalls 67,000+ cases of Power Stick deodorants sold at Walmart, Dollar Tree, and Amazon due to manufacturing violations. Check lot numbers now.

The Food and Drug Administration has issued a recall of more than 67,000 cases of Power Stick deodorant products. The antiperspirant deodorant items are made by A.P. Deauville, a company based in ...