The Food and Drug Administration (FDA) has been busy lately with various recalls. One involved Power Stick deodorant and ...

Sarepta Therapeutics is pausing shipments of its gene therapy for muscular dystrophy following several patient deaths that ...

The FDA and Power Stick recalled thousands of deodorant cases because manufacturing practices did not comply with FDA ...

The Food and Drug Administration has identified a Class I recall of certain lots of Medline Industries Craniotomy ...

The Food and Drug Administration on Monday named a longtime pharmaceutical executive to run the agency's drug program, the latest in a string of leadership changes at the agency.

Pennsylvania-based A.P. Deauville, LLC is recalling several types of its Power Stick deodorant, due to a process issue.

Thursday’s authorization, following a multiyear FDA review, has come under scrutiny, including from Yolanda Richardson, ...

The U.S. Food & Drug Administration announced the ongoing recall of multiple varieties of deodorant. Keep reading to learn the specific deodorant packaging and scents that were recalled, plus other ...

The FDA's assessment of the bread recall has designated it as a Class II risk, which means the product "may cause temporary ...

Genox LyondellBasell New Material Co. Ltd. is using mechanical recycling processes for the material.

The Food and Drug Administration’s (FDA) Psychopharmacologic Drugs Advisory Committee (PDAC) voted 10-1 against the approval of brexpiprazole in combination with sertraline for the treatment of adults ...

The debate over whether to use hormone therapy to treat menopausal women continues, as a Food and Drug Administration (FDA) expert panel weighs in. The panel, consisting […] ...