A U.S. judge in West Virginia said no to a consumer class action lawsuit for Digitek heart meds.
Litigation began in 2008, after Digitek's manufacturer Actavis Totowa discovered 20 double strength pills from a New Jersey plant and recalled a whole batch. Plaintiffs also sued distributor Mylan Pharmaceuticals, three of its subsidiaries, and distributor UDL Laboratories.
Some plaintiffs claimed personal injuries, including wrongful death, while others claimed economic losses.
The judge found that among the six cases, none of the cases were similar. Some of the plaintiffs claimed to be injured by Digitek but were never seen by doctors.
Plaintiffs sought new glasses, toll charges, insurance premiums, the cost of two enemas.
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