FDA Requests Removal of All Ranitidine Products (Zantac) from …
The U.S. Food and Drug Administration today announced it is requesting manufacturers withdraw all prescription and over-the-counter (OTC) ranitidine drugs from the market immediately.
Zantac Recall | FDA Removal of Zantac (Ranitidine) Products
Sep 9, 2019 · Manufacturers issued a recall of all ranitidine Zantac products because the drugs may contain N-Nitrosodimethylamine (NDMA), a cancer-causing chemical. Sandoz was the first company to issue a voluntary generic Zantac recall on Sept. 24, 2019.
FDA Updates and Press Announcements on NDMA in Zantac (ranitidine)
FDA has advised companies to recall their ranitidine if testing shows levels of NDMA above the acceptable daily intake (96 nanograms per day or 0.32 parts per million for ranitidine).
Sanofi Provides Update on Precautionary Voluntary Recall of Zantac …
Oct 23, 2019 · As a precautionary measure, Sanofi on Friday, October 18, intiated a voluntary recall of all Zantac OTC (over-the-counter) in the United States. This includes Zantac 150®, Zantac 150® Cool Mint,...
The FDA Announces Two More Antacid Recalls Due to Cancer Risk
Jan 10, 2020 · Two more companies recalled their ranitidine drugs, generic forms of Zantac, over concerns they may contain a carcinogenic substance.
Ranitidine (Zantac) recall expanded, many questions remain
Update: On April 1, 2020, the FDA requested manufacturers to withdraw all prescription and over-the-counter (OTC) ranitidine drugs (Zantac, others) from the market immediately, due to the presence of a contaminant known as N-Nitrosodimethylamine (NDMA).
Zantac and other heartburn drugs recalled over possible cancer …
Apr 1, 2020 · The move from the Food and Drug Administration Wednesday applies to all prescription and over-the-counter versions of ranitidine, best known by the brand name Zantac.
Popular heartburn drug ranitidine recalled: What you need to …
Oct 1, 2019 · If you or a family member take ranitidine (Zantac) to relieve heartburn, you may have heard that the FDA has found a probable human carcinogen (a substance that could cause cancer) in it. The story is unfolding quickly and many details remain murky. Here is what we know so far and what you should do.
FDA announces more recalls of antacids containing traces of …
The Food and Drug Administration has recalled several more lots of heartburn medications, including more generic versions of Zantac, that have been found to contain trace amounts of a substance...
Zantac Lawsuit Update – Forbes Advisor
Feb 21, 2024 · A recall is when the Food and Drug Administration requires all of a product be pulled from shelves. The FDA simply requested that all retailers stop selling Zantac and ranitidine products....
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