The Food and Drug Administration has expanded its recall of the blood pressure drug valsartan for the third time. On July 5th the European Medicines Agency issued an alert that Chinese-made valsartan contained a probable carcinogen called NDMA. At that time 22 European countries were impacted by the valsartan recall. Over the last month, the valsartan recall disaster has spread around the world.

FDA Warns | Then Updates and Updates Again:

A week later on July 13th the FDA announced a recall of several drug products containing the contaminated valsartan. The FDA updated its recall notification on July 17th and again on July 27th and again on August 2nd that additional companies were involved.

Do you get the sense that this evolving valsartan recall disaster keeps evolving? Now we see that the FDA has added valsartan to its Drug Shortages list on August 3, 2018!

We’re not surprised. The generic industry has consolidated. That means there are fewer manufacturers making raw ingredients and finished products. A great many of them are located abroad.

If large company develops a problem in China or India it can affect the supply of your medicines at a local Walgreens or CVS. We suspect that quite a few pharmacists are calling around looking for safe valsartan.

What Companies Are Involved in the Valsartan Recall Disaster?

According to the FDA here are some of the companies affected:

  • Teva Pharmaceuticals labeled as Major Pharmaceuticals
  • Prinston Pharmaceutical Inc. labeled as Solco Healthcare LLC.
  • Teva Pharmaceuticals USA labeled as Actavis
  • AvKARE
  • Remedy Repack
  • A-S Medication Solutions LLC
  • Bryant Ranch Prepack Inc.
  • Lake Erie Medical, doing business as Quality Care Products LLC
  • NuCare Pharmaceuticals Inc.
  • Northwind Pharmaceuticals
  • H J Harkins Company
  • Proficient Rx LP
  • Northwind Pharmaceuticals

Here is a list of the actual products affected. The FDA updated this list on August 8, 2018.

We wrote about the worrisome implications of the valsartan recall disaster at this link. We fear that the FDA’s ability to monitor generic drug manufacturing in countries like China and India leaves a lot to be desired. The FDA itself admits that:

“The amounts of NDMA found in the recalled batches of valsartan exceeded these acceptable levels. The agency wanted to put some context around the actual potential risk posed to patients who used versions of valsartan that may have contained high levels of NDMA. Based on records from the manufacturer of the recalled valsartan, some levels of the impurity may have been in the valsartan-containing products for as long as four years.”

That’s right…”as long as four years.”

How Are Americans affected by the valsartan recall disaster?

Hundreds of thousands of patients are likely impacted by this recall mess. Pharmacists will be trying to find people uncontaminated valsartan. Others will likely be switched to drugs in the same class. They include:

Irbesartan

Losartan

Olmesartan

Telmisartan

Take Home Questions:

We find this whole valsartan recall disaster worrisome for several reasons. How did this problem persist for four years without the FDA detecting it? Are there other ticking time bombs out there that the FDA hasn’t even considered?

How can Americans trust the Food and Drug Administration to protect them from foreign-made pharmaceuticals? The FDA’s inspection process is very different in other countries. For one thing, the agency has to notify the governments and the companies well in advance of an inspection. In the U.S., FDA inspections are unannounced.

Learn more about these and other concerns by listening to our recent podcast. You can listen to the streaming audio or download the mp3 file for free at this link.

Share your own thoughts about the valsartan recall disaster in the comment section below.

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