Is your medicine safe? Discover which medications are affected by Glenmark & FDC's massive US recall!

In the world of healthcare, the medicines we rely on play a central role in keeping us healthy and feeling our best.

But what happens when these trusted products start raising concerns?

Recently, many Americans have been left asking this very question after learning about recalls from two major drug companies—Glenmark Pharmaceuticals and FDC Ltd.—for products sold in the US.


These recalls were prompted by manufacturing issues and have been reported by the US Food and Drug Administration (USFDA).

Here at The GrayVine, we are dedicated to keeping you informed about important health and safety updates, and this one is no exception.

Let's take a closer look at the details of these recalls and what they mean for you.


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Stay informed: Glenmark and FDC Ltd's recent recalls remind us of the importance of safety in the medications we trust. Image Source: Pexels / Julie Viken.


Glenmark's hypertension medication recall

Glenmark Pharmaceuticals, which is based in Mumbai, India, has found itself in a difficult situation with its US subsidiary, Glenmark Pharmaceuticals Inc.

The company has issued a recall for certain batches of Carvedilol tablets, which are commonly prescribed to treat high blood pressure and heart failure. The affected strengths are 25 mg and 12.5 mg.

The recall stems from the discovery of an impurity known as N-Nitroso Carvedilol I (NNCI-I) at levels exceeding the FDA's recommended limits.


While the risk of serious health consequences is low, this impurity could potentially cause harm if present in significant amounts.

As a result, this recall has been classified as Class II, indicating that any adverse health effects would likely be temporary or reversible.

The recall, which began on January 22, serves as a reminder of the importance of stringent quality control in the pharmaceutical industry.


FDC's glaucoma treatment recall

FDC Ltd is also recalling a significant number of products: 118,104 bottles of Timolol Maleate ophthalmic solution USP, used in the treatment of glaucoma.

The recall was initiated on January 23 and is the result of a "defective container" issue. In this case, patients are unable to properly extract the solution due to the cap's spike being lodged in the nozzle.

This recall, also classified as Class II, emphasizes the critical role that packaging plays in ensuring the safe and effective use of medications—especially those used to treat serious conditions like glaucoma.


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Check your eyedrops: If you're using Timolol Maleate ophthalmic solution, make sure to verify its packaging after the recall. Image Source: Unsplash / Getty Images.


Also read: Is it safe to eat honeycomb? Here's what you need to know

The impact on patients and the healthcare system

These recent recalls are an important reminder of the complexities involved in the production and distribution of medications.

They also highlight the importance of staying informed about the medicines we use.

For patients, it is essential to remain vigilant and keep an eye out for recall notices, as well as to contact healthcare providers if affected by these issues.


Fortunately, the USFDA plays a crucial role in monitoring pharmaceutical safety and acting to protect public health.

For anyone impacted by the recalls, reaching out to healthcare providers for alternative treatments and returning any affected medications is essential.

Pharmacies and healthcare professionals are on high alert and ready to assist patients through this process, ensuring treatment continues as safely and smoothly as possible.


Source: YouTube / News 19 WLTX.​


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Key Takeaways

  • Glenmark Pharmaceuticals and FDC Ltd are recalling products from the US market due to manufacturing issues.
  • Glenmark is recalling specific batches of Carvedilol tablets because of unacceptable levels of a nitrosamine impurity.
  • FDC Ltd is recalling bottles of Timolol Maleate ophthalmic solution because of a defective container preventing the solution from being dispensed.
  • These recalls are classified as Class II by the USFDA, implying that the products may lead to temporary or medically reversible adverse health consequences.

Here at The GrayVine, we understand how unsettling news about medication recalls can be. Have you or a family member been impacted by these recent recalls? How do you stay updated on the safety of the medications you take? We’d love to hear from you in the comments below!

Read next: You won’t believe why this passenger had to give up their seat on a flight!
 
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