FDA duloxetine recall 2024: More than 7,000 bottles recalled
23 hours ago · FDA recalls more than 7,000 bottles of antidepressant over a possible cancerous chemical ... Download USA TODAY's app to get to the heart of news Green onions recalled in 11 states over salmonella ...
Recalls, Market Withdrawals, & Safety Alerts | FDA
The list below provides information gathered from press releases and other public notices about certain recalls of FDA-regulated products. Not all recalls have press releases or are posted on...
TreeHouse Foods Announces Voluntary Recall of Certain Waffle …
OAK BROOK, Ill., Oct. 18, 2024 /PRNewswire/ -- TreeHouse Foods, Inc. (NYSE: THS) is voluntarily recalling certain frozen waffle products listed below due to the potential to be contaminated with ...
Thousands of duloxetine bottles, an antidepressant sold as ... - CBS News
1 day ago · The recall covers 7,107 bottles of duloxetine, the FDA said. The bottles include 500 delayed-release 20mg capsules. The lot number is 220128, with an expiration date of 12/2024.
FDA Egg Recall May Have 'Serious' Health Effects: Avoid These …
Oct 10, 2024 · The Food and Drug Administration has escalated its ongoing recall of eggs due to salmonella contamination to the most serious class.
FDA announces recall of heart pumps linked to deaths and injuries
Apr 16, 2024 · A pair of heart devices linked to hundreds of injuries and at least 14 deaths has received the FDA's most serious recall, the agency announced Monday.
Drug Recalls | FDA - U.S. Food and Drug Administration
Visit Recalls, Market Withdrawals, & Safety Alerts for all FDA-regulated products. Follow FDA Recall Information on X (formerly Twitter).
FDA says 561 deaths tied to recalled Philips sleep apnea machines
Feb 4, 2024 · The Food and Drug Administration says 561 deaths have been reported in connection to recalled Philips devices to treat obstructive sleep apnea and other breathing disorders.
Why are there so many listeria food recalls? - Quartz
1 day ago · It has been a very busy year for food recalls in the United States. The U.S. Food and Drug Administration (FDA) and the U.S. Department of Agriculture (USDA) announced several recalls over the ...
US FDA Identifies Recall of ResMed's Respiratory Devices as Most …
Jan 11, 2024 · (Reuters) - The U.S. Food and Drug Administration (FDA) on Thursday classified the recall of certain respiratory masks made by ResMed as most serious as their use could cause major injuries...