Mushrooms sold across two states have been recalled over fears they could be harboring listeria, a bug that "can cause ...

The U.S. Food and Drug Administration raised concerns over ink printing potentially running when exposed to high temperatures ...

Prestige Consumer Healthcare Inc. issued a voluntary recall for more than 10,000 cases of honey cough syrup on June 17.

The Class I recall status indicates that the product poses a risk of causing serious health consequences or death if consumed ...

Your morning coffee ritual is usually a simple pleasure, but a recent recall of certain coffee pods might make you ...

U.S. Food & Drug Administration (FDA) warning letter to a prominent wellness product and services company offers a blunt reminder ...

Oncologic Drugs Advisory Committee (ODAC) voted against the overall benefit/risk profile at the proposed dosage of GSK plc’s ...

FDA issues warning letters to distributors of food, dietary supplements and unapproved drugs that contain ...

Whoop pushed back on the warning letter, claiming its blood pressure feature for a wearable wristband is for “wellness” and ...

The FDA claims the wearable tech company's BPI offering is 'adulterated' and 'misbranded,' and is being sold without the proper regulatory approvals.

The Food and Drug Administration said Wednesday it has expanded existing warnings on the two leading COVID-19 vaccines about a rare heart side effect mainly seen in young men.

The warning reflects growing concern over a surge in opioid products marketed to US consumers containing concentrated levels of 7-hydroxymitragynine (7-OH).