On February 4 a subcommittee of the House Committee on Oversight and Reform issued a scathing report alleging baby food manufacturers were marketing products they knew contained “dangerous levels of toxic heavy metals.” A statement from the subcommittee’s chairman, Representative Raja Krishnamoorthi of Illinois, said,…
In the fall of 2019 the USDA reported on the existence of NDMA in Zantac and generic ranitidine products Several months later an order was issued requiring the recall of every single ranitidine drug on the market. The discovery of this contaminent in Zantac was…
The distressing discovery of NDMA in Zantac has brought class-action lawsuits on behalf of plaintiffs who claim the companies knew of the presence of NDMA in the medication yet did not disclose that information to the FDA. In the United States District Court’s Southern District…
Sun Pharma became the seventh and latest manufacturer to join the metformin recall parade after finding high levels of a potential cancer-causing contaminant NDMA. The company announced in late September it was voluntarily recalling 1 lot of its metformin hydrochloride for extended-release (ER) oral suspension…
A man who developed bladder cancer after taking Zantac for nearly 30 years is suing the drug’s manufacturers, saying they knew the product was dangerous yet kept it on the market. The filing claims the plaintiff’s cancer was caused by N-Nitrosodimethylamine (NDMA), a potent carcinogen…
In a blow to Johnson & Johnson, a federal judge has ruled that the talc lawsuits may continue after approval of the expert witnesses in the case. J&J faces more than 16,000-talc related lawsuits nationwide, the majority of which are pending before U.S. District Judge…
Pinellas County Schools is now the fourth school district in Florida to join a nationwide lawsuit against e-cigarette manufacturer Juul. According to the Tampa Bay Times, the School Board voted unanimously on April 14 to join nearly 100 other school systems around the country…
In the latest step of a major investigation, the U.S. Food and Drug Administration has determined that prescription and over-the-counter (OTC) ranitidine medications, including Zantac, may expose consumers to “unacceptable levels of impurity.” As a result, the FDA is requesting that manufacturers withdraw all ranitidine…
According to the United States Drug Enforcement Agency, which tracks the path of every single pain pill sold in the United States, 76 billion oxycodone and hydrocodone pain pills were sold from 2006 through 2012. During this growing drug epidemic manufacturers increased production about…
The United States Food and Drug Administration announced last fall that they had confirmed the presence of NDMA, a potential cancer-causing chemical, in Zantac and its generic counterpart, ranitidine. Since the FDA announcement hundreds of lawsuits have been filed against drug makers. Sanofi-Aventis…
