what attorney do i contact on losartan recall

Why did losartan get recalled?

If you or a family member has suffered cancer after taking Losartan, contact a knowledgeable defective drug lawyer today at the Willis Law Firm. We can quickly provide you with an absolutely FREE legal evaluation of your case and advise you on your prospects for a successful Losartan cancer lawsuit. Your free case review comes with no obligation to you and is entirely …

Should I talk to a lawyer about my losartan case?

Sep 24, 2019 · On Sept. 23, 2019 the Food and Drug Administration issued a voluntary nationwide recall of a popular and widely-prescribed blood pressure medication due to a cancer-related contamination.. Five lots of the generic drug called losartan have …

Can I sue for cancer caused by losartan?

Joe Lyon is a highly-rated Cincinnati, Ohio product liability attorney and Losartan lawyer investigating Losartan recall lawsuits and cancer risks for plaintiffs nationwide. The Lyon Firm has experience engaging pharmaceutical companies following recalls …

Which drugs have been recalled by the FDA?

Losartan Recalls Due to NMBA In September 2019, Torrent Pharma expanded a recall for Losartan after tests detected a cancer-causing impurity called NMBA. In April 2019, Torrent Pharmaceuticals Ltd. announced a voluntary recall for Losartan Potassium Tablets USP and Losartan Potassium/Hydrochlorothiazide tablets, USP due to the detection of the ...

Is there a class action lawsuit against losartan?

Losartan Class Action Lawsuit Seeks Compensation for Buyers of Recalled Drugs. The makers of numerous batches of recalled generic losartan face a class action lawsuit, which says that contaminated versions of the hypertension drug sold in recent years were worthless, due to the presence of cancer-causing impurities.May 29, 2019

Can you sue for recall medication?

Can You Sue Even If the Drug That Harmed You Was Not Recalled? Yes. In some cases, drugs that have not been recalled still cause injuries or harm over and above a reasonable level of risk. Bad drug claims are very complex and are often pursued in the form of large class-action suits.

How serious is the losartan recall?

Sandoz Canada and Sanis Health are recalling all lots of prescription losartan tablets due to the presence of an azido impurity above the acceptable limit. The impurity is a mutagen and can create a heightened cancer risk over time if allowed to rise above certain levels.Sep 17, 2021

What is the latest recall on losartan?

In November, the FDA announced a voluntary recall of losartan potassium/hydrochlorothiazide, 100 mg/25 mg tablets in 1,000-count plastic bottles, NDC 0781-5207-10, Lot number JB8912, Exp. Date 06/2020.

How do I know if my losartan has been recalled?

To find out if your medication has been recalled, check if the recalled drug name and associated manufacturer match those on the label of your prescription. Then, check to see if your drug's NDC and lot number match as well. If you can't find the information on your medication, contact your pharmacy.Oct 3, 2019

Is losartan no longer available?

Rising discontinued losartan in August 2019. Sandoz discontinued losartan in 2020. Torrent discontinued losartan tablets in late-2021.

What happens when a medication is recalled?

If the recall involves an over-the-counter drug, stop taking it at once. You can return the product to the place of purchase and ask for a refund -- stores generally have return and refund policies when a recall has been issued. Your doctor or pharmacist can recommend an alternative medicine to use during the recall.Jan 16, 2022

What to do if a medication is recalled?

If a prescription medication that you have been taking is recalled, do not panic. Stop taking the medication immediately, and call your doctor or contact a pharmacist and ask for a recommended replacement. Read the available materials from the FDA or the manufacturer to understand the reason for the recall.May 21, 2020

Is losartan still on recall 2021?

PD-Rx Pharmaceuticals Inc. is recalling 576 bottles of losartan potassium tablets because they contain trace amounts of the nitrosamine impurity NMBA, according to the May 5, 2021, US Food and Drug Administration (FDA) Enforcement Report.

Is losartan still on recall 2020?

The affected lots of the voluntary recall by Legacy Pharmaceutical Packaging are the following: NDC 68645-494-54, losartan potassium tablets USP 50 mg, 30 count, Legacy Lot 180190, expires on 10/2020. NDC 68645-494-54, losartan potassium tablets USP 50 mg, 30 count, Legacy Lot 180191, expires on 10/2020.Sep 25, 2019

Is losartan manufactured by Aurobindo recalled?

The discovery has led to a global recall of hundreds of lots and millions of bottles of the commonly prescribed blood pressure meds valsartan, losartan and Irbesartan.Jul 2, 2019

Should I be worried about taking losartan?

It comes with serious risks if you don't take it as prescribed. If you don't take it at all: Losartan lowers high blood pressure. If you don't take it, your blood pressure will stay high. High blood pressure increases your risk of a stroke or heart attack.

What can I take instead of losartan?

TelmisartanTelmisartan, also available as brand-name Micardis, has better 24-hour coverage than losartan.Like the other ARBs, telmisartan comes in convenient combination tablets: telmisartan/HCTZ and telmisartan/amlodipine.Telmisartan is equally as effective as olmesartan at lowering blood pressure.More items...•Mar 15, 2019

What blood pressure medication has been recalled 2021?

Lupin discontinued the marketing of Irbesartan and Irbesartan and HCTZ tablets in January 2021, the FDA noted. The FDA says Irbesartan and hydrochlorothiazide tablets are packaged in 30- and 90-count bottles and were distributed nationwide in the U.S. to wholesalers, drug chains, mail order pharmacies and supermarkets.Oct 20, 2021

Does losartan cause ear ringing?

Change in sensation of taste. Cough. Sensation of ringing or other noise in the ears (tinnitus). Inflammation of the pancreas (pancreatitis).Mar 24, 2017

Is losartan manufactured by camber recalled?

In February 2019, Camber Pharmaceuticals, Inc. voluntarily recalled 87 lots of losartan potassium tablets. ... Several repackaged Camber and Torrent products have also been recalled. N-nitroso N-Methyl 4-amino butyric acid (NMBA) is a potential human carcinogen.Sep 20, 2019

How to contact a lawyer for Valsartan?

Contact a Valsartan Cancer Lawyer if: 1 You have been diagnosed with a qualifying cancer at least ONE YEAR after taking Valsartan or a contaminated Losartan. If you are unsure whether your medication was contaminated or not, contact an attorney to assist in reviewing the National Drug Code records. 2 You have a diagnosis of: kidney cancer, liver cancer, colon cancer, stomach cancer, or intestinal cancer 3 You have been diagnosed with cancer AFTER 2014 4 You were taking Losartan or Irbesartan for at least one year prior to cancer diagnosis 5 You have received recall letter OR have drug records with a recalled NDC number. 6 If you have NOT received a recall letter, please order your drug records dating back to 2014 to current

Why is there a recall on losartan?

The recalls are due to impurities from N-Nitroso-N-methyl-4-aminobutyric acid (NMBA), as well as NDMA and NDEA, which are classified as a potential human carcinogen.

How much did Merck settle Vioxx?

The FDA ultimately recalled the medication. Merck settled the outstanding Vioxx claims for $4.85 billion following multiple trials in both state and federal courts.

Who makes the recalled meds?

The recalled tablets were manufactured by Hetero Labs Ltd. in India and distributed by Camber Pharmaceuticals. Camber has not received any reports of adverse events related to the recalled drugs, though cancer risks are clearly a concern.

Is NDMA a carcinogen?

NDMA has no approved uses in the United States, and the chemicals NDEA and NBMA also have carcinogenic properties. Toxicologists agree the dose and duration of NDMA exposure determines if a Valsartan patient’s cancer can be attributed to the contaminated drug.

Why was Losartan recalled?

Certain blood pressure drugs containing Losartan were recalled because they may contain a carcinogenic impurity that could potentially raise a user’s risk of cancer.

Does Losartan help with diabetes?

Losartan is a generic medication that treats high blood pressure (hypertension) and helps protect the kidneys from damage due to diabetes (nephropathy). Losartan can also lower the risk of strokes in patients with an enlarged heart.

What is NMBA in medicine?

N-Nitroso-N-methyl-4-aminobutyric acid (NMBA) These are toxic chemicals that are left over as an impurity in the final drug. The carcinogens are generated in the manufacturing process — and specifically when drug-makers reuse certain materials, such as solvents.

Why was Losartan recalled?

In November of 2018, drug manufacturer Sandoz voluntarily recalled Losartan after the FDA notified the maker that the drug was tainted with unsafe levels of probable home carcinogens. Since the first recall, dozens more have followed.

What is the generic name for Cozaar?

Losartan is the generic form of Cozaar, a popular hypertension drug. It belongs to the family of angiotensin II receptor antagonists (ARB), which includes Valsartan and Irbesartan. These drugs work by blocking the angiotensin II receptor, which creates an enzyme that restricts the blood vessels. With the vessels wider and more relaxed, ...

Who is the FDA investigating for Losartan?

The FDA investigation into Losartan manufacturers began when the FDA cited Zhejiang Huahai for producing pharmaceuticals with 20 times the limits considered safe by the FDA. After the warning regarding the unsafe levels of MNBA and NDMA, Zhejiang Huahai continued distributing hazardous products.

Is Losartan safe for humans?

The Food and Drug Administration notified several companies that the generic Losartan they were produc ing contained impurities that made them unsafe for human consumption. Upon notice from the FDA, many of the makers voluntarily recalled their products.

Who is the plaintiff in the Losartan lawsuit?

In New Jersey, four plaintiffs, Glenn Roddey, a Florida resident, Helen Johnson, a Florida resident, Alicia Degracia, a California resident; and William Kolacek, an Illinois resident, filed a lawsuit against makers of Losartan alleging they knowingly sold the drug with unsafe levels of probable human carcinogens.

Is Losartan a carcinogen?

Due to their business nature, these manufacturers should have been aware that the process used to create Losartan creates organic compounds that are probable human carcinogens. Quality control measures should have been in place to test the content of NMDA, NDEA, MNBA, and other hazardous chemicals.

Is Losartan a lawsuit?

As a result of the drug contaminations and recalls, numerous lawsuits are pending against Losartan manufacturers. While producers of the contaminated drugs have been quick to comply with FDA recall suggestions, patients unknowingly consumed these prescriptions for years without knowing the potential risk.

Check If Your Blood Pressure Medicine Was Recalled

The FDA has created a list of recalled blood pressure drugs and will update it as more information becomes available from ongoing testing. If you take Losartan, you should check the list periodically, as recalls may expand and information may change.

Losartan Recalls

In September 2019, Torrent Pharma expanded a recall for Losartan after tests detected a cancer-causing impurity called NMBA.

What is Losartan?

Losartan is a medication that is mainly used to treat high blood pressure (hypertension). It is also used for heart failure, left ventricular heart enlargement, and preventing kidney damage due to diabetes.

What is the Problem?

Drug-makers have recalled a small amount of blood pressure medications containing Losartan because they were contaminated with dangerous levels of a toxic chemical that causes cancer. The chemical, N-nitrosodiethylamine (NDEA), is an impurity that was left over from the industrial processes used to manufacture Losartan.

Hyzaar Recall

November 2018 — Sandoz Inc. recalled 100-mg/25-mg tablets of Hyzaar (Losartan and Hydrochlorothiazide) due to the presence of NDEA.

Blood Pressure Drug Recalls

Recalls have also been issued for blood pressure drugs containing Valsartan and Irbesartan due to carcinogenic impurities.

What are NDEA, NMBA, and NDMA?

There are 3 types of cancer-causing impurities that have led to recalls for blood pressure drugs:

What is the Losartan recall?

The losartan recall is for a fairly small portion of the losartan drugs distributed in America: under 1% of the national losartan drug inventory. Even so, many people have received the contaminated drugs and must be protected from possible harmful losartan side effects such as cancer.

Is Losartan a generic?

Along with volsartan and irbesartan, losartan is another generic high blood pressure drug that’s been found to have an impurity which can cause cancer. This dangerous drug defect has led to a losartan recall announced by the U.S. Food and Drug Administration and can be the basis of a losartan cancer lawsuit by victims of the defective drug.

Is Valsartan recalled?

Generic versions of certain blood pressure medication drugs sold as losartan, valsartan and irbesartan all have been found in recent months to include harmful impurities which can cause cancer. These are the drugs recalled by the FDA in the latter half of 2018. Valsartan was the first BP med in this group to be recalled.

Is Losartan a BP?

However, later it was learned that losartan, too, could have cancer-causing impurities, which led to the drug having a losartan recall of its own. Losartan is a generic form of medications Hyzaar and Cozaar. It is a BP medication -- or hypertension drug -- whose active ingredients have been produced by Lek Pharmaceuticals in Ljubljana, Slovenia. ...

Is N-nitrosodiethylamine a carcinogen?

Unfortunately, NDEA, or N- nitrosodiethylamine, is believed to be carcinogenic, or cancer-causing. In fact, it’s been classified as a probable carcinogen for humans by the International Agency for Research on Cancer (IARC).

Is NDEA a carcinogen?

The World Health Organization also has classified NDEA as a Group 2A carcinogen, meaning it is a probable human carcinogen. Keep in mind that NDEA isn’t just an impurity which can arise in drugs as a byproduct during manufacturing. NDEA also can be found in tobacco smoke -- which, in itself, can cause cancer.

When was Losartan approved?

Then, in 2010, the FDA approved a generic version of losartan. Losartan, along with other drugs taken for treatment of high blood pressure, are known as ARB drugs, or angiotensin II receptor blockers.

Is Losartan a drug?

Losartan Lawsuit. Losartan is one of the 10 most prescribed drugs in the United States. As a treatment for high blood pressure, losartan is considered an important drug in battling heart disease around the world. The World Health Organization even named losartan one of its essential medications — those that satisfy a vital need for the public.

Why was Valsartan recalled?

This prompted the first recall of valsartan medicines due to the presence of a cancer-causing substance called N-nitrosodimethylamine (NDMA) in July 2018.

What is Losartan used for?

Losartan is the generic name of a drug used to treat hypertension. It belongs to a family of medications called angiotensin II receptor blockers (ARBs). They are also known as sartans and AT1 receptor antagonists. Other drugs in this family include valsartan, irbesartan, and candesartan. The drug works to treat high blood pressure by blocking ...

When was the first angiotensin II antagonist developed?

The very first angiotensin II antagonist was developed in the early 1970s. However, it was not suitable as a drug, so scientists started looking into developing something more viable. Eventually, Losartan became the first successful angiotensin II antagonist drug in 1986. By 1995, the U.S. Food and Drug Administration had approved the drug for use in the United States.

Who makes losartan?

Losartan was originally sold under the trade name Cozaar and was marketed by Merck. Eventually, other ARBs were developed using losartan as a basis. In 2010, the patent ran out on the drug and the first generic formulations of losartan potassium tablets were approved by the FDA.

Does Losartan help with high blood pressure?

By blocking the effects of angiotensin II, blood vessels are allowed to widen and relieve the pressure of the blood. If left unchecked, high blood pressure can lead to heart attack, heart failure, kidney damage, stroke, vision loss, sexual dysfunction, and more. Although losartan is best known as a treatment option for high blood pressure, ...

Does Losartan cause back pain?

According to Cozaar’s official prescribing information sheet, clinical trials for Losartan have revealed common side effects that occur more frequently in those taking Cozaar versus those taking a placebo. These include dizziness, upper respiratory infection, nasal congestion, and back pain.

Why was blood pressure medication recalled?

The recall was prompted by the discovery of cancer-causing impurities in the medications .

When was Zantac recalled?

The heartburn drug Zantac and several generic versions of the drug were recalled due to contamination in September 2019. Read more about the Zantac recall >>>.

Is Valsartan recalled?

In July 2018, valsartan was the first blood pressure drug recalled. Valsartan is a similar blood pressure medication to losartan. A recall on losartan medications soon followed. Manufacturers recalled hundreds of lots of generic losartan over the course of the next year.

What is the name of the drug that blocks blood vessels?

Losartan is an angiotensin II receptor blocker (ARB). An ARB is a type of blood pressure drug. It works by keeping a person's blood vessels unconstricted, thereby preventing pressure from building. Losartan is sold under the brand name Cozaar. It can also be found in generic forms.

Can you stop taking losartan?

Do not stop taking your recalled losartan medication. High blood pressure can be life-threatening. Do not discontinue your medication without consulting a healthcare professional. Doing so can lead to serious health risks.