US Rep. DeLauro Reintroduces Device Safety Bill To Remove PMA Product Liability Suit Protections

A US House representative and two co-sponsors have reintroduced the Medical Device Safety Act, which would remove the defense against state product liability suits for premarket-approved devices from the Federal Food, Drug, and Cosmetic Act (FDCA).

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The Medical Device Safety Act Act would invalidate a February 2008 Supreme Court ruling cementing preemption from liability suits for PMA-approved devices • Source: Brenda Sandburg

A bill to remove liability protections for device-makers whose products are premarket-approved by the Food and Drug Administration was reintroduced in the House on 10 May by Rep. Rosa DeLauro, D-CT.

The Medical Device Safety Act, H.R. 2669, would expand access to legal recourse for individuals who have been injured...

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