The FDA deemed the Keurig recall a Class II, which means that "use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences," but the likelihood of ...
Keurig Dr Pepper voluntarily recalled 80,640 McCafé decaf K-Cup pods sold in California, Indiana and Nevada after FDA ...
Some coffee drinkers may need to check their McCafé Premium Roast Decaf Coffee K-Cup Pods after over 80,000 pods were ...