While the FDA recall happened over a year ago, the statute of limitations for people who were diagnosed with cancer before the Zantac recall is in 2022. For those who believe they may have a case ...

With Zantac, however, the high levels of NDMA are far greater than the maximum set by the FDA." Those who take medicine containing ranitidine should consider switching drugs, as the levels of NDMA ...

The product pulls were reported in a recent edition of the U.S. FDA's weekly enforcement report, which catalogs recalls after they ... (NDMA) in Zantac led to mass product pulls and lawsuits ...

The FDA reports that the recall was initiatiated after it was ... including angiotensin II receptor blockers (ARBs), ranitidine, nizatidine, and metformin—have recently been recalled because ...

Cucumbers potentially contaminated with salmonella could cause "serious adverse health consequences or death," the FDA warned.

Systane eye drops were recalled earlier this week after the company discovered a fungal contamination in one of its products.

Rising Pharmaceuticals, who the FDA reported issued a voluntary recall on Nov. 19, did not immediately respond to USA TODAY's request for comment. New study:Ultra-processed foods may increase fat ...

Precedent set by the Supreme Court may well be turned on its head – at least as far as FDA drug and vaccine approvals go ... The case (involving allegations that Zantac causes cancer) is now on appeal ...

A voluntary recall was initiated after it was discovered that pre-mixed Bloody Marys may contain undeclared allergens, including fish (anchovy), or soy.

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 ...

The Food and Drug Administration (FDA) announced a nationwide recall of a popular single-use eye drop on December 23. Alcon ...