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Notification regarding the recall of Dilantin (Phenytoin Sodium Injection) due to discolored product caused by incorrect stoppers. The action was taken following customer complaints and involves a
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How to fill out dilantin injection recall notification
How to fill out Dilantin Injection Recall Notification
01
Start by gathering all necessary information, such as patient ID, lot number of Dilantin injection, and any other relevant details.
02
Clearly fill out the 'Patient Information' section with the patient's full name and other required details.
03
In the 'Recall Information' section, provide the specifics of the recall including the reason and any possible effects.
04
Document the actions taken prior to this notification, such as contacting the patients or healthcare providers.
05
Review the completed form for accuracy and ensure all sections are filled out appropriately.
06
Submit the notification form to the relevant agency or authority as directed.
Who needs Dilantin Injection Recall Notification?
01
Healthcare providers who administer Dilantin injections.
02
Patients currently prescribed Dilantin injections, particularly those using affected lots.
03
Pharmacies that dispense Dilantin injections.
04
Medical institutions that stock Dilantin injections.
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What is Dilantin Injection Recall Notification?
Dilantin Injection Recall Notification is a formal communication issued by the manufacturer or regulatory authority to inform healthcare providers and patients about a health risk associated with Dilantin Injection, often due to quality control issues or safety concerns.
Who is required to file Dilantin Injection Recall Notification?
Manufacturers, distributors, and healthcare providers who have distributed or administered Dilantin Injection are required to file a Dilantin Injection Recall Notification.
How to fill out Dilantin Injection Recall Notification?
To fill out the Dilantin Injection Recall Notification, one must complete the designated form by providing essential details such as product name, lot numbers, reason for recall, affected quantities, and any actions taken to notify customers.
What is the purpose of Dilantin Injection Recall Notification?
The purpose of Dilantin Injection Recall Notification is to promptly inform relevant parties about potential risks or adverse effects related to the medication, ensuring patient safety and minimizing harm.
What information must be reported on Dilantin Injection Recall Notification?
The information that must be reported includes the product name, lot number, expiration date, reason for the recall, affected quantities, distribution details, and contact information for further inquiries.
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