FDA Recalls More Generic Blood Pressure Meds: Where Are Your Medications Manufactured?

In July of 2018, the FDA made a series of voluntary recalls of several versions of the generic blood pressure medication valsartan which were made in China and were contaminated by the “possible carcinogen,”  N-nitrosodimethylamine (NDMA).
At the time I asked readers the question, “Is your BP med made in china and is it safe?” as it became clear that now in the US users of medications must be very aware of the source and quality of the products they put in their body.
Generic prescription medications and OTC products are highly likely to be manufactured out of the US and with minimal oversight.
Since then the FDA has announced multiple other recalls for companies producing angiotensin II receptor blockers (ARBs) in the same class as valsartan, including products containing losartan and irbesartan,. These drugs have been found to be contaminated contaminated with NDMA or another carcinogen  N-nitrosodiethylamine (NDEA).
The recall now includes irbesartan and losartan plus additional lots of valsartan. Thus, some patients who we switched from valsartan to losartan are now having to switch again.
Click the following links to review updated lists of irbesartan products under recall, losartan medications under recall, valsartan products under recall and valsartan products not under recall.
Here’s  the FDA’s valsartan alert notice from 1/2/19

FDA is alerting patients and health care professionals to Aurobindo Pharma USA’s voluntary recall of two lots of valsartan tablets, 26 lots of amlodipine and valsartan combination tablets, and 52 lots of valsartan and hydrochlorothiazide (HCTZ) combination tablets due to the amount of N-Nitrosodiethylamine (NDEA) in the valsartan active pharmaceutical ingredient. Aurobindo is recalling amlodipine and HCTZ only in combination medications containing valsartan. Neither amlodipine nor HCTZ is currently under recall by itself.
Aurobindo is recalling lots of valsartan-containing medication that tested positive for NDEA above the interim acceptable daily intake level of 0.083 parts per million.
The agency continues to investigate and test all angiotensin II receptor blockers (ARBs) for the presence of NDEA and N-Nitrosodimethylamine (NDMA) and is taking swift action when it identifies these impurities that are above interim acceptable daily intake levels.
FDA also updated the list of valsartan products under recall and the list of valsartan products not under recall.
FDA reminds patients taking any recalled ARB to continue taking their current medicine until their pharmacist provides a replacement or their doctor prescribes a different medication that treats the same condition. Some ARBs contain no NDMA or NDEA.

Fortunately, there are multiple generic  and brand nameARBs we can substitute for the recalled products.

Patients Discover How Hard It Is To Find Non-Chinese Medications

When I tried to find the source of my generic medications, the results were eye-opening:

 my cholesterol drug is made in India by an Indian company and my blood pressure drug is made in Columbus, Ohio, by a Jordanian company.

I had not realized how globalized the pharmaceutical industry had become.
Many readers also researched the source of the pills they were taking and shared their experience through comments on my blog:
“Frustrated” wrote

My cardiologist changed my blood pressure med to irbesartan. Another generic ARB. I went to get it filled today at a local grocery store pharmacy. I asked where it was made and they showed me the bottle. Guess what? It was SOLCO/Prinston as distributor and Zhejiang Huahai Pharmaceuticals LTD – the same manufacturer as the tainted valsartan. Exactly the same. Despite the recent horrible FDA inspection report of that facility which is posted online here: https://www.fda.gov/downloads/Drugs/GuidanceComplianceRegulatoryInformation/CDERFOIAElectronicReadingRoom/UCM621162.pdf
Also, the FDA has found another cancer causing chemical in the drug since I last wrote – now there are two. I checked at [MAJOR CHAIN] pharmacy – they use the SAME CHINESE MANUFACTURER. I checked at [MAJOR CHAIN 2] – yep, they use the SAME CHINESE MANUFACTURER. This is really starting to get scary. I’m trying hard to find a pharmacy that has the non-Chinese version (there are 16 other generic manufacturers of the drug). My insurance company only permits me to use the pharmacies I tried today. Funny how everyone is buying Chinese. Does that validate the claims made in the Epoch article. Is this really that Chinese are undercutting everyone else? I’m just disgusted. I will tell you that if I owned a pharmacy I would not purchase my generics from the same company that just caused one of the largest drug recalls in history. It must be really really cheap. Really really cheap.

Mitch writes:

I have been taking Losartan, but became really concerned with the latest news about carcinogens found in two more BP medications. I called EVERY local pharmacy, including big-box stores, grocery store pharmacies, independent pharmacies, and traditional pharmacies. Not a single one has US-made losartan. Every one of them has stock of meds made in either China or India. One pharmacists told me that he had no control of what he sells; it’s all decided on the corporate level. Another said that he would stock the cheapest generic he could find. Still another pharmacy tried to convince me that Citron, Torrent, and Solco are New Jersey companies selling US-made drugs. It takes only a few minutes of Internet research to prove them wrong. Apparently, there is no incentive to stock US-made drugs. I agree, the consumers have to take action and write to their representatives demanding answers from the FDA.

BIS wrote:

I have just had the same experience. My Indian made Valsartan (Camber) was recalled so my doctor switched me to Irbesartan 150 mg tablets which at my local CVS were also manufactured by Camber. I reluctantly took these while searching for US or European made alternatives. I just went to CVS to get my refill. When I got home instead of the Indian Irbesartan I received a bottle manufactured by Zhejiang Huahai Pharmaceutical Co. Ltd.,(ZHP) Xunqiao, Linhal, Zhejiang China. I am a mechanical engineer not a chemistry major but I believe Irbesartan contains API which is what has been the problem from this company. Looking at the internet I see that the FDA has and import alert for this company. The import alert halts all ZHP-made API and finished drug products using the company’s API from legally entering the United States (https://www.pharmacist.com/article/fda-places-zhejiang-huahai-pharmaceuticals-import-alert). Let’s see- did the Chinese use good API in this batch….I called the CVS and asked for alternatives and was told “good luck”. My doctor said he will work with me if I can find non Chinese or Indian medication. I go out of my way to buy American made goods as I have worked in manufacturing my entire career and have made numerous trips to China and seen what goes on. My Chinese colleagues when they come to the US fill their bags with US made baby formula and vitamins (which probably contain Chinese ingredients). If anyone finds a US or European source of BP medication please post it.

What Can We Do?

One of my readers, Kate, made the following suggestion which made a lot sense:

write to the Senate committee that oversees the FDA. Demand more clarity in labeling of prescription bottles – the country of origin should be CLEAR and CONSPICUOUS – just like that little “Made in China” sticker on the photo above – but on the prescription label itself. Right now only the pharmacist’s supply bottle has the labeling. Write your congressman and to:
U.S. Senate Committee on Health, Education, Labor & Pensions
428 Senate Dirksen Office Building
Washington, DC 20510

I would encourage patients who are taking these recalled ARBS (which are really good blood pressure medications) to check their pill bottles and check with their pharmacists to determine if they have been recalled. If the pharmacist can’t replace your medication with an identical ARB that hasn’t been withdrawn, ask your physician for one of the alternatives listed above.
Find out what country you’re generic drugs in general are made in and let your congressional representatives know you want better FDA oversight of off-shore pharmacuetical manufacturing along with complete transparency with respect to country of origin.
Skeptically Yours,


6 thoughts on “FDA Recalls More Generic Blood Pressure Meds: Where Are Your Medications Manufactured?”

  1. I know this blog last updated in 2019. I don’t think the situation is getting better. I just pick up my mom losartan from a major chain. Guess what manufacturer on the label? Solco Huahai. I know this company was the bad guy who makes up this mess. However, FDA lifted the import ban on Nov 2021. Should we trust the FDA and this solco company? All other chains in my area only carry Solco. I don’t know what else to do. Thanks

  2. I am quite disgusted. I take 200 mg of Losartan Potassium a night for diabetic neuropathy. After the December recall from Torrent, CVS sent another recall announcement in March. Today I went to fill a new prescription; even with insurance the brand cozaar is prohibitively expensive. The store dispensed torrent generic, which upon returning home I saw the bottle numbers were on the list of recalled items they previously had sent.

  3. This is really serious. I have been switched from Valsartan to Losartan, and now Irbesartan. I took the tainted Solco/Prinston Valsartan for three years. After switching to Irbesartan, it was recalled. I feel like I’m running from poison pill to poison pill. And just when I get a new one, that starts to get recalled. Yesterday (March 1, 2019) there were more Losartan lot recalls announced. I wrote to every senator on the FDA oversight committee and to my local congressman, and my two senators. And what did I get? Nothing. Not a single response. In my view, this situation is the beginning of a national emergency. So many people are taking these generics from overseas, and these chemicals they are finding (NDEA, NDMA and now N-Methylnitrosobutyric acid (NMBA)) are all VERY nasty cancer-causing poisons. At some point, I think that the major pharmacies in the US selling this garbage and the insurance companies that stand by and require people to buy the cheapest generic garbage they can find, begin to bear some responsibility. They are on NOTICE that these drugs are contaminated. And yet, they continue to sell this garbage. Last fall, after going into a [MAJOR CHAIN] and finding Solco/Prinston Irbesartan on their shelf AFTER the FDA banned further imports (because of the Valsartan generic disaster caused by the same company), I wrote to the [MAJOR CHAIN’s] headquarters essentially saying, guys you are selling a drug by a company that has been banned from further shipment into the US. The response I got was essentially (in writing) well, we can sell the remaining supply and that particular item is not on recall (which was true at the time). Less than two months later, Solco/Prinston Irbesartan was recalled for NDEA contamination. You can see that here: https://www.fda.gov/Safety/Recalls/ucm629627.htm
    So I wrote back to the headquarters of [MAJOR CHAIN] and brought this to their attention. I told the author of the prior letter that they should have known better and that likely additional patients took this tainted medication because they chose to continue selling it. Shame on them. As you might expect, I received no reply.
    After my exhaustive research and following all this, I have come to the following conclusion. In my opinion, it’s all about the money. Insurance companies demand cheaper generics so they can earn more profits. Yet our premiums keep going up. Foreign drug companies, like the one in China that started all this, can cut corners without the same oversight as in the US or Europe. Further, the FDA response to this disaster has not been fast enough. There is absolutely no reason that drug companies cannot test their lots of drugs for these chemicals and quickly pull the bad ones. Yet, almost 8 months later, we’re still seeing recalls. Why does it take 8 months to test pills? FDA should ban further sales of any Irbesartan, Losartan, and Valsartan unless the manufacturer has certified that it has tested all of its lots for these three chemicals. Rolling recalls are not helpful. BAN THIS GARBAGE.
    Because it is about the money, NOTHING WILL CHANGE unless consumers ASK THEIR PHARMACIST to see the manufacturer’s label and where the drug was made (NOT where the distributor is based). Solco/Prinston is the US distributor for the Chinese company ZHP. Nice cover, but consumers must educate themselves and REFUSE to buy Chinese generics. Consumers must call their insurance plans and DEMAND that they cover alternative drug manufacturers. Stop buying your drugs from pharmacies that stock this garbage. And finally, WRITE your congress person and your senators. Without outcry, nothing will be done.

  4. Thanks for the continued heads-ups on contaminated meds. My Irbesartan is made by a company in India… presumably ok— til we find out it’s not!

  5. I was special ordering the Sandoz brand Losartan HCT from CVS. It is manufactured in Ljubljana, Slovenia. I liked it because it was made in Europe rather than India or China. Now guess what? That drug was recalled by the FDA as well for the presence of the same carcinogen.


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