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Document Date: 2011-09-29 19:10:40

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File Size: 324,86 KB

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City

Washington / D.C. / /

Company

FDA’s / Voluntary Medical Device / Overseeing / /

Country

United States / /

/

Event

Product Recall / Product Issues / FDA Phase / /

Facility

See Pub / Institute of Medicine / /

IndustryTerm

risk devices / highrisk devices / unsafe medical devices / unsafe medical device / manufacturing practices / marketed device / device / adequate assurance that devices / unsafe devices / /

MedicalCondition

rare diseases / injury / illness / /

Organization

Food and Drug Administration / Institute of Medicine / U.S. Senate For Release / Congress / US Federal Reserve / FDA / United States Government Accountability Office / Special Committee on Aging / /

Person

Marcia Crosse / Kohl / Corker / /

/

Position

Governor / Chairman / Director / recall coordinator / /

Product

percent / market / strategy / Postmarket Safety Efforts Statement / data / While FDA / classes / Recall Enterprise System / firm / firm of the assigned recall classification / III / classification schemes / highestrisk / notifications firms / devices / risk levels / classifications / device / firms / Premarket Review / termination request / Federal Food / GAO-09-190 / /

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