FDA, recall

FDA sets highest risk level for popular pancake and waffle mix recall
The U.S. Food and Drug Administration issued the highest risk classification to its Pearl Milling Company pancake and waffle mix recall. The Quaker Oats Company initially issued a recall on Jan. 14 for its two pound boxes of the Pearl Milling Company Original Pancake & Waffle Mix due to an undeclared milk allergen, per a press release.
Quaker Oats’ recall on product elevated to highest FDA level due to risk of ‘death’
Quaker Oats’ recall on product elevated to highest FDA level due to risk of ‘death’ - The two-pound boxes of pancake mixe were recalled last month because they may have contained undeclared milk
Pretzel Recall Update as FDA Sets Highest Risk Level'
Consuming the recalled pretzels if you have a milk allergy could cause "serious adverse health consequences or death."
Pancake mix recall skyrockets to highest risk level after FDA warns of milk allergen
The original recall has since been upgraded to Class I, which denotes the highest risk level in connection to a pulled product that could potentially be fatal
FDA increases risk level of granola bar recall due to ‘adverse health’ effects
The U.S. Food and Drug Administration (FDA) has elevated the risk of a recall of various granola bars. In its latest weekly update, the FDA shared the update about a recalled batch of MadeGood granola bars,
Quaker Oats pancake mix recall upgraded to highest risk level over threat of ‘life-threatening allergic reaction’
The Quaker Oats Company, a subsidiary of Pepsi Co, previously announced the limited recall of certain boxes of Pearl Milling Company Original Pancake & Waffle Mix on Jan. 14.
Healio18h
FDA accepts IND for allogenic CAR T-cell therapy that could bypass lymphodepletion
The FDA has accepted an investigational new drug application for ALLO-329, an allogeneic chimeric antigen receptor T-cell ...
manilatimes23h
Press Release: Dupixent sBLA accepted for FDA priority review for the targeted treatment of bullous pemphigoid
Dupixent sBLA accepted for FDA priority review for the targeted treatment of bullous pemphigoid. If approved, Dupixent would be the first and only targeted medicine to treat BP in ...
Managed Healthcare Executive4d
FDA Approves Gomekli, First and Only NF1-PN Treatment for Both Children and Adults
Gomekli is the second ever FDA-approved treatment for rare tumor disease, NF1-PN and the first to be approved for both adult ...
Healio1d
FDA approves GSK’s pentavalent meningococcal vaccine
The FDA approved GSK’s pentavalent meningococcal vaccine to protect children and young adults aged 10 to 25 years against ...
U.S. News & World Report6d
Senators Call on FDA to Act Against Misleading Weight-Loss Drug Commercials
that these products are not FDA-approved." The commercial appears to be taking advantage of a perceived loophole in federal law regarding promotions of compounded drugs by telehealth companies, ...
Targeted Oncology7d
FDA Grants 510(k) Clearance to Ibex Prostate Detect AI for Prostate Cancer
The FDA has granted a 510 (k) clearance to the Ibex Prostate Detect software (formerly Galen Second Read). The Ibex Prostate ...
Pharm Exec13d
FDA Grants Fast Track Designation to Adicet Bio’s CAR T-cell Therapy for Systemic Lupus Erythematosus
The FDA has granted Fast Track Designation to Adicet Bio’s ADI-001, an allogeneic gamma delta CAR T-cell therapy, for ...
Trump administration cuts reach FDA employees in food safety, medical devices and tobacco products
The Trump administration’s effort to slash the size of the federal workforce reached the Food and Drug Administration this ...