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 provides a searchable list of recalled products.
Recalls, Market Withdrawals, & Safety Alerts | FDA - U.S. Food and Drug …
Oct 1, 2024 · 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...
Duloxetine recall: FDA expands recall to more than 233,000 bottles
Dec 13, 2024 · More than 233,000 bottles of an antidepressant have been recalled by public health officials due to a chemical containing the risk of cancer. The U.S. Food and Drug Administration classified...
Drug Recalls, Withdrawals & Warnings (FDA Alerts) - Drugs.com
Jan 24, 2025 · Get the latest up-to-date information on FDA drug recalls, withdrawals, and warnings. Subscribe to alerts by email, app notification, or news feeds.
Alvogen Issues Voluntary Nationwide Recall for One Lot of …
Jan 31, 2025 · Alvogen, Inc. is voluntarily recalling one lot of Fentanyl Transdermal System 25 mcg/h transdermal patches to the consumer level. The reason for the recall is that there is a potential that...
ADHD medication recalled over drug mix-up, bottles may have …
Jan 30, 2024 · A pharmaceutical company is recalling medication for ADHD (attention deficit hyperactivity disorder) and narcolepsy because packages of the drug may contain the wrong pills, the U.S. Food and...
Drug Recalls: Why They Happen and What You Should Do - WebMD
Mar 31, 2024 · A drug recall occurs when a prescription or over-the-counter medicine is removed from the market because it is found to be either defective or potentially harmful. Sometimes, the makers of the...
FDA recalls thousands of antidepressant duloxetine bottles - The Hill
Oct 23, 2024 · The Food and Drug Administration (FDA) issued a Class II recall of more than 7,100 bottles of the antidepressant duloxetine due to the possible presence of a carcinogen.
Another Blood Pressure Medication Has Been Recalled Due to …
Dec 17, 2024 · If you’re one of the 116 million Americans that Cleveland Clinic data suggests have been diagnosed with high blood pressure, the U.S. Food and Drug Administration (FDA) has a warning that one particular blood pressure medication …
Over 110,000 Bottles of Popular Blood Pressure Medication Recalled
Nov 21, 2024 · Last month, on October 23, the U.S. Food and Drug Administration (FDA) recalled 112,770 bottles of one popularly prescribed ACE inhibitor, Ramipril, produced by Lupin Pharmaceuticals Inc., a Baltimore, MD-based company.