Endo's Expanded Clonazepam Recall: Safety Precautions and Actions
Endo Inc. Expands Voluntary Recall of Clonazepam ODT
Endo, Inc. (OTCQX: NDOI) has recently announced the expansion of its voluntary recall concerning Clonazepam Orally Disintegrating Tablets, USP due to potential mislabeling of product cartons. This proactive step aims to ensure patient safety and address concerns about miscommunication regarding the drug's strength.
Understanding the Issue with Clonazepam ODT
Endo's investigation has revealed that some product lots may contain cartons labeled with incorrect strength information and National Drug Code (NDC) due to an error on the part of a third-party packaging vendor. It’s crucial to note that the blister strips and tablets inside these cartons maintain correct labeling reflecting the actual strength of the medication.
Detailed Recall Information
The recall specifically includes several lots of Clonazepam ODT, which are intended for various therapeutic uses including treatment for seizures and panic disorders. Each lot number in question has been documented, reflecting the potential discrepancies in product labeling. Consumers should review any prescribed medication in their possession carefully.
Risks Associated with Mislabeling
Mislabeling poses risks to both children and adults who may consume a dose of Clonazepam ODT that does not correspond with their prescribed treatment. Symptoms resulting from an incorrect dosage may include significant sedation, confusion, or dizziness. In particular, individuals with existing respiratory conditions could face life-threatening consequences if inadvertently administered an incorrect dose.
Current Status of Reports
As of now, Endo has not received any reports of adverse effects stemming from this recall. The company emphasizes its commitment to monitoring safety and responding swiftly to any concerns raised by healthcare providers or patients.
Packaging Details for Clonazepam ODT
Clonazepam ODT is packaged in cartons that include 60 tablets, organized into ten blister strips with six tablets each. The packaging should clearly indicate the drug's name, strength, lot number, expiration date, and NDC number, further confirmed by the previous marketing entity. This meticulous approach to labeling is intended to safeguard both consumers and healthcare providers.
What To Do If You Have the Affected Medication
Consumers who possess any of the recalled Clonazepam ODT lots should cease use immediately and return the product to the place of purchase. Endo is coordinating with wholesale distributors and retailers to ensure the safe return of the recalled products. It’s essential for them to stop any distribution immediately to mitigate potential health risks.
Next Steps for Patients
In the event of inadvertent consumption of the incorrectly labeled Clonazepam, patients are advised to consult their healthcare provider for guidance. Safety is a priority for all patients, and Endo encourages proactive communication between patients and practitioners.
Contact Information for Questions
Patients or consumers who have questions about this recall can reach out to Endo by telephone during business hours. They should seek guidance on how to safely dispose of the product or understand any next steps regarding their treatment.
About Endo Inc.
Endo is a diversified pharmaceutical company dedicated to transforming medical insights into life-enhancing therapies. Their passionate team collaborates to develop and deliver essential medications, ensuring that they can help patients lead their best lives. For further information about their offerings and patient services, visit the Endo website or connect on social media platforms.
Frequently Asked Questions
What prompted Endo to expand the recall of Clonazepam ODT?
The recall was expanded in response to findings that certain cartons contained mislabeling regarding the strength and NDC code, potentially putting patients at risk.
How can patients check if their medication is affected?
Patients should check their Clonazepam ODT packaging for lot numbers listed in the recall announcement.
What actions should consumers take if they have the recalled product?
Consumers should stop using the affected Clonazepam ODT immediately and return it to the point of purchase for a safe return process.
Are there any reported adverse effects from this product recall?
To date, Endo has reported no adverse events associated with the recalled Clonazepam ODT lots.
Who can consumers contact for more information?
Consumers can reach Inmar, the returning distributor, by telephone for inquiries regarding the product recall and for assistance with product return details.
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