FOX 13 Tampa Bay1h
FDA recalls cheese sold at Aldi locations in 4 states
Pouches of Aldi’s Happy Farms shredded Colby Jack cheese have been recalled in four states over concerns they contained metal ...
WWAYTV33h
Canned green beans distributed by Target given 2nd-highest FDA recall classification
The U.S. Food and Drug Administration has assigned its second-highest classification to an earlier recall involving some ...
Medical Device Network on MSN1d
FDA tags Becton, Dickinson and Company infusion software recall as Class I
Problematic software has been the cause of multiple infusion pump recalls in the medical device industry over the past few ...
FDA Approves Expanded Use Of Novartis Rare Disease Drug As Only Treatment For Rare Type Of Kidney Disease
Novartis' Fabhalta receives FDA approval for C3 glomerulopathy, expanding its kidney disease portfolio as global regulatory ...
Targeted Oncology1d
FDA Grants Orphan Drug Designation to PEP-010 in Pancreatic Cancer
The FDA granted an orphan drug designation to PEP-010 for the treatment of patients with metastatic pancreatic cancer.
FOX 4 News Dallas-Fort Worth1d
Nearly 200,000 Target brand canned vegetables under FDA urgent recall due to 'foreign object'
Hundreds of thousands cans of Good & Gather vegetables were recalled after a "foreign object" led the Target Corporation to file an urgent, voluntary recall.
Fierce Pharma1d
J&J advances Stelara succession scheme with FDA nod for Tremfya in Crohn's disease
With another inflammatory bowel disease (IBD) approval in the bag for Tremfya, Johnson & Johnson continues to make good on ...
Target faces urgent recall for 200K cans of vegetables: FDA
Nearly 200,000 cans of Target-brand green beans have been urgently recalled in several states. That’s according to an enforcement report released by the Food and Drug Administration (FDA). On February ...
Potato chips recalled, FDA updates the health risk level for consumption
The U.S. Food and Drug Administration updated the health risk level for a potato chip brand recalled in February.
Medtronic recalls aneurysm-treating device linked to four deaths
The FDA recall affects more than 25,000 of the Fridley-run company’s devices and follows reports of 17 injuries.
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 MacroglobulinemiaFirst-in-class ...
The American Journal of Managed Care7d
FDA Approves Expanded Indication of Eculizumab for Pediatric Generalized Myasthenia Gravis
The FDA first approved eculizumab for use in adult patients with generalized myasthenia gravis in 2017, before expanding the ...