The anxiety-reducing drug, Clonazepam, has been recalled after a potentially "life-threatening" label mix-up, the FDA said in the recall.

The US Food and Drug Administration said taking wrong dose of Clonazepam could result in ‘significant sedation, confusion, dizziness, diminished reflexes, ataxia, and hypotonia’

Endo USA has expanded its voluntary recall of clonazepam orally disintegrating tablets due to a mislabeling issue that could lead to patients accidentally ingesting the wrong dosage. The recall affects several lots of clonazepam ODT in various strengths, including 2 milligram, 1 milligram, 0.25 milligram and 0.125 milligram, which were distributed to retail pharmacies nationwide, according to an Nov. 19 news release from the FDA. The issue stems from cartons being printed with incorrect strength and National Drug Code numbers, although the blister strips and tablets inside the packaging are correct. This mislabeling could result in individuals consuming higher doses of clonazepam, increasing the risk of dangerous side effects including significant sedation, confusion, dizziness and potentially life-threatening respiratory depression. Endo has not received any reports of adverse events associated with the recalls. Consumers with the affected product are urged to discontinue use immediately and consult a healthcare provider.