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FDA Warns Consumers Not to Use Certain Powdered Infant Formula Produced in Abbott Nutrition’s Facility in Sturgis, Michigan

Today, the U.S. Food and Drug Administration announced it is investigating consumer complaints of Cronobacter sakazakii and Salmonella Newport infections.

Making Sense of COVID-19 Booster Recommendations

On September 23, the Centers for Disease Control and Prevention (CDC) officially recommended a booster shot for individuals age 65 and older, as well as those between the ages of...

Alzheimer's Drug Aduhelm FAQ

On June 7, the FDA granted accelerated approval for aducanumab (Aduhelm), the first drug approved to treat Alzheimer’s disease since 2003. However, there is limited evidence that this treatment will...

FDA Requests Removal of all Ranitidine Products (Zantac)

The FDA announced it is requesting manufacturers to withdraw all prescription and over-the-counter (OTC) ranitidine drugs from the market immediately.

What to Know about At-Home COVID-19 Testing Kits

At this time, the FDA has not authorized the sale of any at-home COVID-19 testing kits to consumers, but several companies announced they will be introducing at-home coronavirus tests.

FDA Requests Withdrawal of Weight-Loss Drug Belviq

FDA has requested that the manufacturer of Belviq, Belviq XR (lorcaserin) voluntarily withdraw the weight-loss drug from the U.S. market because a safety clinical trial shows an increased occurrence of...

FDA Product Recall: Medtronic Recalls MiniMed Insulin Pumps for Incorrect Insulin Dosing

The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death.

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