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Opioid Drug Mix-Up Announced By FDA

The Food and Drug Administration has issued a warning that pills, tablets or caplets of Percocet and eight other opioid products packaged by Novartis for Endo Pharmaceuticals may have been mixed up with one drug being packaged as another.

The error is most likely due to improperly cleared packaging machinery in the processing plant. This may have resulted in pills from one product to be carried over into containers of another product. The FDA is not issuing a recall, instead deciding on a warning to consumers.

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