Metformin er 500 mg recall

Attention Metformin users: We want to inform you about an important recall regarding Metformin ER 500 mg tablets. Please read the following information carefully to ensure your health and safety.

What is the recall about?

The Metformin ER 500 mg recall is due to potential levels of N-Nitrosodimethylamine (NDMA) above the acceptable limit set by the U.S. Food and Drug Administration (FDA). NDMA is classified as a probable human carcinogen, which means long-term exposure to high levels of NDMA can increase the risk of cancer.

Which products are affected?

This recall affects specific lots of Metformin ER 500 mg tablets manufactured by certain pharmaceutical companies. To check if your medication is included in the recall, please refer to the lot number and manufacturer details provided on the packaging or consult your healthcare professional.

What should you do?

If you are currently taking Metformin ER 500 mg tablets that are included in the recall, it is important to stop using them immediately. Contact your healthcare provider to discuss alternative treatment options. Do not discontinue or change your medication without consulting a healthcare professional.

Where can you get more information?

For further information about the Metformin ER 500 mg recall, you can visit the FDA's website or contact the respective pharmaceutical company directly. It is crucial to stay informed and take necessary actions to safeguard your health.

Remember, your health is our top priority. Stay informed, stay safe!

Important Information for Patients: Recall of Metformin ER 500 mg

Attention patients taking Metformin ER 500 mg: It has come to our attention that certain batches of this medication have been recalled due to concerns over potential contamination. We urge you to check the packaging and batch number of your medication and take the necessary precautions.

What is Metformin ER 500 mg?

Metformin ER 500 mg is a prescription medication used to control blood sugar levels in patients with type 2 diabetes. It belongs to a class of drugs called biguanides and is typically taken orally, usually once or twice daily.

Why has it been recalled?

The recall of certain batches of Metformin ER 500 mg has been initiated due to the presence of a contaminant called N-nitrosodimethylamine (NDMA), which is classified as a probable human carcinogen. Prolonged exposure to NDMA above certain levels may increase the risk of cancer.

What should you do if you have been taking Metformin ER 500 mg?

If you have been taking Metformin ER 500 mg, we recommend checking the packaging and batch number of your medication. You can find this information on the label of the bottle or container. If your medication is part of the recall, please contact your healthcare provider immediately for further guidance.

Is there an alternative medication available?

If your medication has been recalled, your healthcare provider will be able to recommend alternative options to manage your diabetes. It is important to continue taking any prescribed medications as directed and to follow up with your healthcare provider for regular monitoring of your blood sugar levels.

In conclusion

The recall of Metformin ER 500 mg is an important matter for patients with type 2 diabetes. If you have been taking this medication, please check the packaging and batch number to ensure you are not using a recalled product. Contact your healthcare provider for further guidance and to discuss alternative treatment options if necessary.

Reason for Recall

Metformin ER 500 mg, a commonly prescribed medication for the treatment of type 2 diabetes, has been recalled due to potential contamination with a cancer-causing agent. The recall was initiated by the manufacturer after independent testing revealed the presence of N-Nitrosodimethylamine (NDMA) above acceptable limits.

NDMA is a known environmental contaminant and can also be found in certain foods, water, and air pollution. It is classified as a probable human carcinogen based on animal studies. Prolonged exposure to high levels of NDMA can increase the risk of developing cancer, especially in the liver, stomach, and intestines.

The recall of Metformin ER 500 mg is a precautionary measure to ensure patient safety. The contamination may be a result of the manufacturing process or storage conditions, and the manufacturer is conducting further investigations to identify and address the source of the problem. In the meantime, it is important for patients taking this medication to be aware of the potential risks and take appropriate action.

If you are currently taking Metformin ER 500 mg, it is recommended to contact your healthcare provider to discuss alternative treatment options. Your healthcare provider can help determine the best course of action based on your individual needs and medical history.

It is important to note that not all Metformin ER 500 mg products are affected by this recall. Patients are advised to check the lot number and expiration date on their medication bottle or packaging to determine if their specific medication is included in the recall. The FDA has also provided a list of affected products on their website for reference.

Patients should not stop taking their medication without first consulting their healthcare provider. Abruptly discontinuing treatment can have negative effects on blood sugar control and overall health. Your healthcare provider can guide you on the appropriate steps to take and may recommend alternative medications or monitoring measures.

If you experience any unusual symptoms or have concerns about your medication, do not hesitate to seek medical attention. Your healthcare provider is the best resource for addressing any questions or concerns you may have regarding the recall of Metformin ER 500 mg.

Implications for Patients

New Prescription

If you are currently taking Metformin ER 500 mg, it is important to contact your healthcare provider as soon as possible. They will evaluate your medical condition and advise on the appropriate course of action. They may prescribe an alternative medication or adjust your treatment plan to ensure that your diabetes is effectively managed.

Monitoring Blood Sugar

While the recall does not mean that all Metformin ER 500 mg tablets are unsafe, it is recommended to monitor your blood sugar more closely. Check your blood sugar levels regularly and keep a record of the results. If you experience any unusual symptoms or fluctuations in your blood sugar, contact your healthcare provider immediately.

Alternative Medications

If your healthcare provider determines that you need an alternative medication, they will discuss the available options with you. There are several other effective medications to manage diabetes, so do not be discouraged. Your healthcare provider will work with you to find a suitable replacement that meets your individual needs.

Stay Informed

It is important to stay informed about the latest developments regarding the Metformin ER 500 mg recall. Follow credible sources, such as the FDA or your healthcare provider, for updates and safety information. By staying informed, you can make well-informed decisions about your health and diabetes management.

Contact Your Pharmacy

Contact your pharmacy to inquire about whether their stock of Metformin ER 500 mg is affected by the recall. They will be able to provide you with the most up-to-date information and guide you on how to proceed. If necessary, they can assist in obtaining an alternative medication or help you navigate the recall process.

Remember: Your health and well-being are of utmost importance. Take action proactively and communicate with your healthcare provider to ensure that your diabetes is properly managed.

What to Do if You Have the Affected Product

1. Stop using the medication

If you have the affected product, it is important to stop using it immediately. The recall has been issued due to the presence of a potential cancer-causing impurity called NDMA. Continuing to use the medication may put your health at risk.

2. Contact your healthcare provider

Reach out to your healthcare provider as soon as possible to inform them that you have the affected product. They will be able to provide guidance on what steps to take next and help you switch to an alternative medication if necessary. It is important to follow their instructions carefully.

3. Check for alternative medications

Your healthcare provider will be able to recommend alternative medications that are safe and effective for managing your condition. They may prescribe a different strength or brand of metformin, or suggest a completely different medication altogether. Be sure to ask any questions you may have about the new medication.

4. Follow the recall instructions

Pay attention to any instructions provided by the manufacturer or regulatory authorities regarding the recall. This may include returning the affected product to the place of purchase, contacting the manufacturer for a refund or replacement, or disposing of the medication in a specific manner. Following these instructions will help ensure your safety.

5. Stay informed

Keep yourself updated on the latest information regarding the recall. Check the FDA or manufacturer's website for any updates or announcements about the recall. Stay in touch with your healthcare provider and ask them to inform you of any new developments or recommendations. Being informed will help you make informed decisions about your health.

Contact Information for Additional Assistance

If you have any questions or concerns regarding the recall of Metformin ER 500 mg, there are several ways you can reach out for additional assistance. Our customer service team is here to help you and provide the support you need.

If you wish to speak with a representative directly, you can call our toll-free hotline at 1-800-123-4567. Our knowledgeable staff will be available to answer any questions you may have and provide guidance on what steps to take next.

Alternatively, you can send an email to [email protected]. Please include your contact information and a brief description of your question or concern, and one of our representatives will respond to you as soon as possible.

If you prefer to visit us in person, our headquarters are located at 123 Main Street, City, State. Our office hours are Monday to Friday, 9:00 am to 5:00 pm. You can stop by during these hours to speak with a representative face-to-face and get any assistance you need.

In addition, we have created a dedicated webpage on our website with important information and updates regarding the recall. You can visit our website at www.metforminrecall.com/recall-updates for the latest news and updates related to the recall.

Remember, your health and safety are our top priority. Please do not hesitate to contact us if you have any concerns or require additional assistance. We are here to support you through this process.