The FDA gave the coffee recall a Class II classification, meaning consumption could cause "temporary or medically reversible ...

The new Keurig recall covers McCafé Premium Roast Decaf Coffee K-Cup pods that may contain caffeine instead of decaf.

Consumers who drink the recalled products could experience “temporary or medically reversible adverse health consequences," ...

The FDA has issued a Class II recall for over 80,000 McCafe coffee pods labeled as decaf that may contain caffeine. Sold in ...

If you have McCafe Premium Roast Decaf Coffee K-Cup Pods at home, you may want to think twice before popping one into your ...

Keurig Dr Pepper voluntarily recalled 80,640 McCafé decaf K-Cup pods sold in California, Indiana and Nevada after FDA ...

The U.S. Food and Drug Administration designated its second highest alert level to the recall.

A voluntary recall has been issued for more than 80,000 Keurig coffee pods, according to the Food and Drug Administration.

(Gray News) — Keurig is recalling about 80,000 McDonald’s-branded K-cups, according to the FDA. The recall is for McCafe Premium Roast Decaf Coffee pods. The FDA said the K-cups are being recalled ...

Keurig coffee pods face recall over major labeling error - The affected coffee pods were distributed in three U.S. states ...

Drug developers secured approvals for 46 new therapeutic agents from the FDA’s Center for Drug Evaluation and Research (CDER) in 2025. This cohort brings the 5-year average down a touch, to 48 new ...

Swedish neurotech startup Flow Neuroscience has secured FDA approval for the first brain stimulation device for home use in treating depression, a regulatory milestone that could reshape a mental ...