The seafood salad may be of particular risk to those customers who have an allergy or severe sensitivity to soy, the FDA has ...

A soup mix recall issued this month has been updated by the U.S. Food and Drug Administration (FDA) as a Class I risk, the ...

In the US, liraglutide, semaglutide, and tirzepatide are currently under investigation for their ability to stimulate weight ...

As previously announced, the Company requested the Meeting in response to the FDA issuing a CRL, dated October 22, 2024, for the Company's Ketamine product's Abbreviated New Drug Application, which ...

The FDA is scrutinising reports of haematological cancers in patients treated with bluebird bio's gene therapy for the rare ...

The FDA has approved updated drug labeling for Sandoz in the treatment of B-cell chronic lymphocytic leukemia.

The affected products contain Listeria monocytogenes, a deadly bacterium that kills around 260 people in the U.S. each year.

The U.S. Food and Drug Administration (FDA) terminated a recall for Berkeley Club Beverages water on November 13 and recently updated the product's recall status. In September, West Virginia-based ...

The FDA updated the fludarabine phosphate injection labeling under Project Renewal, clarifying the dosage for combination ...

Pending the FDA’s decision, compounding pharmacies will remain free to make and market versions of the blockbuster ...

DentalMonitoring performed an extensive clinical study program on over 2,650 patients across 29 sites in North America, which ...