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ARTICLE · 03 FEBRUARY 2021

Zantac MDL Narrowed By Two Preemption-Based Dismissal Orders

Winston Taylor
Explore more from Winston Taylor

In re: Zantac (Ranitidine) Product Liability Litigation is a coordinated multi-district litigation (MDL) centralized in the Southern District of Florida. The MDL involves allegations (which the ...

United StatesConsumer Protection
Christopher B. Essig
Christopher B. Essig
Scott M. Ahmad
Scott M. Ahmad

In re: Zantac (Ranitidine) Product Liability Litigation1 is a coordinated multi-district litigation (MDL) centralized in the Southern District of Florida. The MDL involves allegations (which the defendants deny) that the active ingredient in Zantac (a heartburn medication) and its generic formulations are potentially carcinogenic because ranitidine can transform into the cancer-causing molecule NDMA. On 2020's final day, the Court issued two dismissal orders that, on federal preemption grounds, eliminated (1) innovator liability claims under 35 jurisdictions' laws against the prescription brand manufacturers by individuals who took generic formulations of those brand manufacturers' products; and (2) all misbranding claims against the prescription generic manufacturers by individuals who took those generic manufacturers' products.2 

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