These strategies can create a healthcare ecosystem that prioritizes patient safety, empowers consumers with information and ...

A recent study identified 157 cardiovascular devices recalled from 2013 to 2022. Recalls were commonly attributed to device ...

An injectable blood pressure drug has been recalled after the FDA has warned it could cause side effects, such as stroke or death.

Here are three recent recalls reported to the FDA: ...

The website changes raise concerns about “the interference of politics with the study and the practice” of science and ...

The U.S. Food and Drug Administration has sent a warning letter to Marlborough, Mass.-based medical technology company ...

The speed control dial on a wheelchair motor medical device has been recalled nationwide following three serious injuries and ...

Amid a deluge of executive actions, the Trump administration has directed federal health agencies to pause external ...

The batch was "intended for quarantine," but was sold by mistake, the FDA said. The FDA set the recall at class 2, the second-highest risk level, and consumers are advised to stop using the ...

The new director of the FDA’s device center contrasted a European rule with the lack of mandatory reporting requirements for ...

The FDA issued a recall for the second-highest recall classification out of three tiers. Here's what we know about why the skin care product was recalled and why. The FDA issued a Class II recall ...