News

FDA Issues Recall in Various States Due to Possible Listeria Contamination
The Food and Drug Administration (FDA) has been busy lately with various recalls. One involved Power Stick deodorant and ...
FDA commissioner stirs debate over hormone therapy for menopause
A Food and Drug Administration (FDA) expert panel has reignited a debate over whether hormone therapy should be used to treat ...
Sarepta shares slide again as drugmaker bows to FDA pressure to pause gene therapy
Sarepta Therapeutics is pausing shipments of its gene therapy for muscular dystrophy following several patient deaths that ...
Popular Deodorant Recalled, Impacts Thousands of Cases Sold Nationwide, FDA Reports
The FDA and Power Stick recalled thousands of deodorant cases because manufacturing practices did not comply with FDA ...
FDA taps new leader for drug program
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.
Over 67,000 Cases of Popular Deodorant Recalled Nationwide, FDA Reports
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 ...
CSP Daily News12h
FDA’s authorization of Juul e-cigarettes prompts mixed responses
Thursday’s authorization, following a multiyear FDA review, has come under scrutiny, including from Yolanda Richardson, ...
The FDA recalled Power Stick deodorant. Here is what to know
Pennsylvania-based A.P. Deauville, LLC is recalling several types of its Power Stick deodorant, due to a process issue.
MPR17h
FDA Panel Votes Against Brexpiprazole Plus Sertraline for PTSD
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 ...
FDA Issues Risk Warning for Bread Recall Update
The FDA's assessment of the bread recall has designated it as a Class II risk, which means the product "may cause temporary ...
Recycling Today12h
LYB joint venture receives FDA nonobjection letters for recycled PP, HDPE processes
Genox LyondellBasell New Material Co. Ltd. is using mechanical recycling processes for the material.
BizPac Review13h
‘All of us are begging’: New push for FDA to remove ‘black box’ warnings from menopause products
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 […] ...