On November 9, 2006, the FDA recalled acetominophen 500 mg tablets produced by Perrigo Company. It is believed that some of these tablets contain metal fragments. The recall includes approximately 11 million bottles. This is an over the counter medication and not a prescription drug.
Drug Recall
On November 9, 2006, the FDA recalled acetominophen 500 mg tablets produced by Perrigo Company. It is believed that some of these tablets contain metal fragments. The recall includes approximately 11 million bottles. This is an over the counter medication and not a prescription drug.
Tags:
Legal
More in Legal
See all
