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Tag Archives: Stryker

Former FDA Director Joins Public Citizen in Device Recall Petition

By Mesh Medical Device Newsdesk |

DECEMBER 23, 2011 ~ The consumer group Public Citizen frequently calls for the recall of dangerous drugs or medical devices including a petition last August calling for the recall of synthetic surgical mesh from the market because of the complication rate and a failure to show a benefit over risk (here). 

Changes Are Afoot in U.S. Medical Device Regulations, Morningstar, August 15, 2011

By Mesh Medical Device Newsdesk |

This excellent article by Morningstar reminds us that the Food and Drug Administration (FDA) has been reviewing the regulatory process that allows most medical devices to make their way into the marketplace and the agency plans to have new changes in place by October. This is sparked by the July release of the Institute [continue reading…]

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