Firm News: Drugs & Devices: Page 14

W&L Accepting Zimmer Persona Knee Replacement Cases

A recent voluntary recall of the porous coated, uncemented Zimmer Persona Knee Trabecular Metal Tibial Plates, which the U.S. Food and Drug Administration (FDA) subsequently categorized as a Class II recall, has led Weitz & Luxenberg, P.C., to begin accepting cases involving Zimmer Persona Knee replacement injuries, the law firm today announced. The company that…

W&L Taking Zimmer Persona Knee Replacement Cases

Weitz & Luxenberg is now investigating cases in which patients suffered harm from use of a Zimmer Persona knee replacement device. The porous coated, uncemented Zimmer Persona Trabecular Metal Tibial Plate was voluntarily recalled on Feb. 16 and was categorized as a U.S. Food and Drug Administration (FDA) Class II recall on March 12. The…

Media, FDA Join W&L in Warning Women of Morcellation Dangers

Expanding news coverage of the cancer-spread risks posed by power morcellators is helping show why women are right to seek compensation from the makers of the surgical devices, Weitz & Luxenberg said.   The most recent reports of injuries to women appeared in The Wall Street Journal, which in late November ran two major stories…

W&L, Allied Firms Obtain Stryker Hip Implants Settlement; Could Top $1 Billion

Stryker Corp. has agreed to pay potentially more than $1 billion to settle claims from patients injured by the company’s Rejuvenate and ABGII modular hip implants, the nationally prominent personal-injury law firm of Weitz & Luxenberg today announced. The settlement capped nearly four months of intensive negotiations between Stryker and Weitz & Luxenberg’s Ellen Relkin…

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