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

The U.S. Food & Drug Administration (FDA) has announced a recall of more than 80,000 coffee pods sold by Keurig Dr Pepper.

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.

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

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

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

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

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

Here’s a list of impacted products.

Indiana is among states affected by the recall of more than 80,000 Keurig K-Cup coffee pods.

Feeling jittery? More than 80,000 Keurig coffee pods labeled decaf have been recalled because they may in fact contain caffeine, an FDA enforcement report said. According to the report Keurig Inc., ...

The McCafé Decaf K-Cups may actually contain caffeine, which can lead to adverse health effects. The FDA gave the recall the ...