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www.fdanews.com/articles/143564-public-citizen-chides-fda-for-failing-to-recall-stryker-stent

Public Citizen Chides FDA for Failing to Recall Stryker Stent

January 30, 2012
Michael Carome, deputy director of Public Citizen’s Health Research Group and author of a petition to recall the Stryker Corporation’s Wingspan stent, boldly criticized the FDA for not recalling the medical device due to evidence of increased possibility of stroke in certain patients when the Wingspan stent was used.
PR Newswire