Complete List of Lot Numbers and What You Need to Know

In the past year, several blood pressure medications have been recalled due to concerns over impurities. One of the most prominent recalls has been for Losartan, a medication used to treat hypertension (high blood pressure). This recall has affected several different lots of Losartan tablets, citing the presence of a potential carcinogen.

If you are currently taking Losartan or know someone who is, it is important to educate yourself about the recall and understand what steps to take to ensure your health and safety. This article will provide a complete list of lot numbers affected by the recall, as well as important information about the potential risks and how to proceed with your medication regimen.

Whether you are a healthcare provider prescribing Losartan to patients or a patient taking it yourself, this article will serve as a useful resource to navigate the Losartan Recall 2019.

What is Losartan?

Losartan is a medication used to treat high blood pressure (hypertension) and to help prevent kidney damage in patients with type 2 diabetes. It belongs to a class of drugs called angiotensin II receptor blockers (ARBs) which work by relaxing blood vessels to lower blood pressure.

Losartan is usually taken orally in tablet form and is typically prescribed in doses ranging from 25 mg to 100 mg, depending on the individual patient’s needs. It can be taken with or without food, but it is important to follow all directions given by your healthcare provider.

Losartan has become a popular medication for treating hypertension and is often prescribed in place of other drugs in the same class because it has fewer side effects. However, recent recalls of losartan have highlighted potential issues with certain batches of the medication, and patients are advised to check the lot numbers of their medication to ensure it is safe to use.

Why has Losartan been Recalled?

Losartan is a medication used to treat hypertension, or high blood pressure. It works by blocking certain chemicals in the body that cause blood vessels to constrict, resulting in a lowering of blood pressure. Losartan has been recalled because it has been found to contain impurities called nitrosamines, specifically N-Nitroso-N-methyl-4-aminobutyric acid (NMBA) and N-Nitrosodimethylamine (NDMA).

These impurities are potentially carcinogenic, which means that they may increase the risk of cancer over time. The U.S. Food and Drug Administration (FDA) has determined that the levels of these nitrosamines found in recalled losartan products exceed safe limits. As a result, several pharmaceutical companies have issued voluntary recalls of their losartan products.

It is believed that the nitrosamine impurities found in losartan are the result of a manufacturing process that was not adequately controlled. While there have been no reports of adverse events related to the recall, the FDA recommends that patients who are taking losartan should speak with their healthcare providers to determine the best course of action.

• If you are taking losartan, check the lot number and expiration date on your prescription label or packaging to see if it is included in the recall.
• If your medication is one of the recalled lots, contact your healthcare provider or pharmacist immediately for advice on what to do next.
• Do not stop taking losartan without consulting with your healthcare provider. Suddenly stopping this medication can lead to serious health complications.
• If your medication is not part of the recall, continue taking it as prescribed, but remain vigilant for any changes in your health or symptoms that may be related to your medication.

It is important to note that not all losartan products have been affected by the recall. The FDA continues to investigate the source of the nitrosamine contamination and is working with manufacturers to ensure that all products are safe for patient use.

Complete List of Recalled Lot Numbers

• 20MG Tablets, 30 count: Lot Numbers JNC1812, JNC1813, JNC1814, JNC1815, JNC1816, JNC1817, JNC1818, JNC1819, JNC1820
• 20MG Tablets, 90 count: Lot Number JNC1820
• 100MG Tablets, 90 count: Lot Numbers JNC1782, JNC1783, JNC1784, JNC1785, JNC1786, JNC1787, JNC1788, JNC1789
• 100MG Tablets, 1000 count: Lot Number JNC1789
• 25MG Tablets, 100 count: Lot Numbers JNC1864, JNC1865, JNC1866, JNC1867, JNC1868, JNC1869, JNC1870
• 50MG Tablets, 90 count: Lot Numbers JNC1806, JNC1807, JNC1808, JNC1809, JNC1810, JNC1811
• 50MG Tablets, 1000 count: Lot Number JNC1811

Note: This list may not be exhaustive and other lot numbers may be recalled. Always consult with your healthcare provider before making any changes to your medication.

What Should You Do if You Have Been Affected?

If you have been taking Losartan medication and believe you may have been affected by the recall, there are a few steps you should take:

1. Contact your healthcare provider: If you have been taking Losartan medication and are concerned about the recall, it’s important to speak with your healthcare provider as soon as possible. They can advise you on the best course of action and may be able to provide you with alternative medication.
2. Check your medication: Look at the lot number and expiration date on the packaging of your medication to see if it matches those included in the recall. If it does, stop taking it immediately and contact your healthcare provider for advice.
3. Return your medication: If your medication has been included in the recall, don’t dispose of it in the trash. Instead, return it to the pharmacy where you purchased it.
4. Keep yourself informed: As the recall continues to unfold, it’s important to stay informed about any updates or changes. Check the FDA website regularly for the latest news, and sign up for alerts if possible.

Remember, if you have been affected by the Losartan recall, it’s important to take action as soon as possible to protect your health and wellbeing. Don’t hesitate to reach out to your healthcare provider or pharmacist for guidance and support.