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

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

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

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

Officials are warning that consuming the coffee product could cause "health consequences." ...