Oyster cracker recall: FDA escalates recall to Class II amid potential presence of 'foreign material'
A food manufacturer is over 15,000 packages of oyster crackers sold at Target, Walmart and other stories due to the discovery ...
The FDA Cracking Down on Compounded Weight Loss Drugs – Here's What It Means for Telehealth Companies and Consumers
After years of weight loss drug shortages, the FDA is saying there's now an adequate supply for most medications and they ...
Clinical Pain Advisor3d
FDA Drug Approval Decisions Expected in April 2025
Treatments for dry eye disease, neuroendocrine tumors, chronic spontaneous urticaria, Barth syndrome, and migraine are under review.
Nationwide Amazon Cookie Recall As FDA Sets Highest Risk Level
The alert affected two types of brands produced by Amazon Fresh, the grocery subsidiary of the top delivery company.
The Manila Times1h
Nurix Announces U.S. FDA Orphan Drug Designation Granted to Bexobrutideg (NX-5948) for the Treatment of Waldenström Macroglobulinemia
Orphan Drug Designation follows positive Phase 1 data presented at the 12th International Workshop on Waldenström ...
FDA recall: 2 popular coffee creamers sold in Mississippi are making people sick. Did you buy?
International Delight coffee creamer sold in Mississippi now under FDA recall. Did you buy them? Are they in your home? What ...
75,000 bottles of coffee creamer recalled by FDA in Ohio, US. See the full list
More than 75,000 bottles of International Delight coffee creamer are being recalled over concerns the product is spoiled.
BioSpace7d
FDA Action Alert: GSK, Alnylam, Sanofi and More
One of the most highly anticipated FDA decisions this month is for Alnylam Pharmaceuticals, which is seeking to expand the ...
Modern Healthcare11d
FDA labels Philips' recall of Tack Endovascular Systems a Class I
Complications with the implant used to treat blood vessel dissection after balloon angioplasty or stent placement can result ...
Pulmonology Advisor11d
FDA Drug Approval Decisions Expected in March 2025
The Prescription Drug User Fee Act (PDUFA) date refers to the deadline set by the US Food and Drug Administration (FDA) for reviewing a New Drug Application (NDA) or Biologics License Application (BLA ...