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 ...

Keurig K-Cups are being recalled nationwide due to a packaging issue that could cause ink to run into the coffee during brewing. The U.S. Food and Drug Administration (FDA) issued a voluntary recall ...

Keurig Dr Pepper recalled McCafé decaf K-Cups that may contain caffeine. Check the UPC and best-by date if you bought them in CA, IN, or NV.