Title: Lupin Pharmaceuticals Recalls Two Batches of Oral Birth Control Due to Reduced Effectiveness
Lupin Pharmaceuticals, a leading pharmaceutical company, has issued a voluntary recall of two batches of their oral birth control product, Tydemy. The recall comes after it was discovered that the pills contained a reduced level of ascorbic acid, which may lead to a decrease in effectiveness, potentially resulting in unexpected pregnancies.
In addition to the decreased ascorbic acid levels, the recalled pills were found to have high levels of a “known impurity.” While the specific impurity has not been mentioned, the presence of such substances can compromise the safety and reliability of the product.
Although the U.S. Food and Drug Administration (FDA) has not received any reports of adverse events associated with the use of the recalled Tydemy pills, Lupin Pharmaceuticals has taken a proactive approach to ensure the well-being of its consumers.
The affected lots, known as L200183 and L201560, were distributed by pharmacies throughout the United States from June 3, 2022, to May 31, 2023. A total of 4,179 boxes of the oral birth control have been recalled. Individuals are advised to check the lot number on the side of the label to determine if their product is part of the recall.
While consumers who are currently taking the recalled batches are instructed to continue taking their pills, they are also encouraged to consult their healthcare providers for an alternative birth control option. It is crucial for individuals to prioritize their reproductive health and explore alternative options to prevent unintended pregnancies.
This is not the first time Lupin Pharmaceuticals has initiated a voluntary recall due to product concerns. Last December, the company recalled certain batches of Quinapril Tablets USP over potential nitrosamine impurity concerns. These proactive measures demonstrate the company’s commitment to prioritizing the safety and well-being of consumers.
As always, it is recommended that consumers stay informed and regularly check for updates from the pharmaceutical company and the FDA regarding any potential recalls or safety alerts for the products they use.
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