Sixteen lots of clonazepam orally disintegrating tablets have been recalled because of a packaging error that could have life-threatening consequences.
Megan Brooks, based in Weston, Connecticut, has been a medical writer/editor for more than 30 years, focusing exclusively on science writing for a professional audience. Megan began her science writing career at Physicians Radio Network , which became Physicians News Network and eventually Reuters Health.
“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, diminished reflexes, ataxia, and hypotonia,” the company said in theespecially for patients with concomitant pulmonary disease, patients who have prescribed dosing near maximal dosing, and patients also taking other medications that could cause additional respiratory depression,” the company warned.
The carton and each blister strip pocket are printed with the name, strength, lot number, expiration date, and NDC number. The blister strips and tablets inside the product pack reflect the correct strength for the lot. The mistake appears on the product cartons. The recalled product lots were distributed through wholesale distributors to retail pharmacies nationwide.
Consumers in possession of any recalled product should immediately stop using it. Any patient who inadvertently took an incorrect dose rather than the intended dose should contact their physician. Questions regarding this recall can be directed to Inmar by telephone at 855-589-1869 or by email at
U.S. Food And Drug Administration United States Food And Drug Administration Fda Blister Bulla Depression Anxiety Ataxia Children Child Childhood Pediatrics Kids Dizziness Panic Disorder Sedation Sedative Sedative Use Seizure
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