Diagnosed with cancer

after taking Zantac?


Zantac has been linked to the human carcinogen  NDMA.

The FDA called for all Zantac to be pulled from the shelves. 

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    Did you or a loved one take Zantac or Zantac OTC?

    Were any of the following cancers diagnosed after exposure to Zantac?

    Zantac Lawsuits: Carcinogen Prompts Recall


    ALERT: April 1, 2020 – “The U.S. Food and Drug Administration today announced it is requesting manufacturers withdraw all prescription and over-the-counter (OTC) ranitidine (Zantac) drugs from the market immediately.”


    Since the 1980s, ranitidine (brand name: Zantac) has been associated with NDMA. While Zantac is not contaminated with NDMA, it contains nitrite (N) and dimethylamine (DMA). Combined, they form the carcinogen NDMA.

    The Food and Drug Administration (FDA) was notified in June of 2019 that routine testing done in Valisure’s labs had linked Zantac to N-nitrosodimethylamine (NDMA).  FDA’s own testing found unacceptable levels of NDMA in Zantac.


    “The results [of several case–control studies and one cohort study] are supportive of the assumption that NDMA consumption is positively associated with either gastric or colorectal cancer.” (World Health Organization)


    On April 1, 2020, the FDA issued a recall on Zantac. In addition to NDMA concerns, “the agency has determined that the impurity in some ranitidine products increases over time and when stored at higher than room temperatures may result in consumer exposure to unacceptable levels of this impurity.”


    If you have been diagnosed with cancer after taking Zantac regularly, please contact us immediately by calling 504-523-2434 or filling out an online Contact Form for a FREE Consultation.

    Possible side-effects include:

    Bladder cancer

    Colon and rectal cancer

    Esophageal cancer

    Intestinal cancer

    Kidney cancer

    Liver cancer

    Lung cancer (non-smokers)

    and more

    Cancer diagnosis after taking Zantac?

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    We handle cases that change lives.


    Peiffer Wolf is committed to making sure that the companies that release harmful drugs or medical devices onto the market are held accountable for their wrongful conduct. Our firm’s Pharmaceutical and Medical Devices practice is led by Attorney Daniel Carr, who has represented thousands of clients from across the United States in cases related to pharmaceutical products and medical devices, including litigations involving Essure, Truvada, Low-T, Xarelto, Pradaxa, ASR hip implants, TVM, Actos, Invokana, Onglyza, and others.


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    Cancer diagnosis after taking Zantac or Ranitidine?