Some Clonazepam Pills Recalled Over Incorrect Doses on Label, F.D.A. Says
The agency warned that adults and children who inadvertently took a higher dose of clonazepam than prescribed could experience side effects, including “significant” sedation, confusion, dizziness, diminished reflexes, the loss of muscle control and muscle weakness.
Popular anxiety drug clonazepam recalled for labeling error
"Children and adults who inadvertently consume a higher dose of clonazepam could be at increased risk for the adverse events of significant sedation, confusion, dizziness, diminis
Clonazepam Recall Grows Over Potentially Life-Threatening Label Error
Sixteen lots of clonazepam orally disintegrating tablets have been recalled because of a packaging error that could have life-threatening consequences.
Anxiety drug clonazepam recalled due to potentially 'life-threatening' labeling error
Clonazepam, an anxiety drug, has been recalled because of a labeling error that could result in harmful consequences.
Clonazepam tablets recalled over ‘life-threatening’ label mistake
A popular anxiety drug is being recalled over a ‘life-threatening’ label mistake. In a recall alert for certain lots of Clonazepam Orally Disintegrating Tablets, the company that produces the tablets has said the medication is mislabeled with the incorrect strength on the carton.
Clonazepam, popular anxiety-reducing drug, recalled nationwide for ‘possibly life-threatening’ error
The anxiety-reducing drug, Clonazepam, has been recalled after a potentially "life-threatening" label mix-up, the FDA said in the recall.
Nationwide Recall of Anxiety Drug Over Life-Threatening Packaging Error
Endo Inc., based in Pennsylvania, has announced a voluntary recall of 16 lots of Clonazepam Orally Disintegrating Tablets after it discovered that a number of cartons may have been printed with the incorrect strength and National Drug Code (NDC) on them.
Recall expended nationwide for clonazepam due to labeling error
Endo, Inc., has expanded its voluntary recall of Clonazepam Orally Disintegrating Tablets, USP (C-IV) due to mislabeled carton strength and NDC numbers caused by a packaging error.
Popular anxiety drug recalled over potentially ‘life-threatening’ issue
The US Food and Drug Administration said taking wrong dose of Clonazepam could result in ‘significant sedation, confusion, dizziness, diminished reflexes, ataxia, and hypotonia’
Popular anxiety drug being recalled nationwide for ‘possibly life-threatening’ error
A popular prescription anxiety drug is being recalled nationwide for a “possibly life-threatening” mistake on the carton. The Pennsylvania-based drug maker Endo announced this week that it is expanding its recall of clonazepam tablets because some cartons bear the incorrect drug strength and wrong drug code.
Anxiety medication recalled for 'life-threatening' labeling error
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.
Clonazepam recall expanded after misprinting on packaging
The company is worried mislabeling could lead to unintentionally taking higher doses and adverse side effects.
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More Clonazepam ODT Recalled Due to Carton Strength Mislabeling
Endo has expanded the recall of Clonazepam Orally Disintegrating Tablets (ODT) to include additional lots that may ...