FDA Requires Transvaginal Mesh Makers To Conduct Safety Studies
Bernstein Liebhard LLP endorses an FDA mandate requiring transvaginal mesh manufacturers to initiate investigations into implant related injuries. New York, New York (PRWEB) January 04, 2012 Bernstein Liebhard LLP reports that on January 3, 2012, the U.S. Food and Drug Administration (“FDA”) ordered Johnson & Johnson and C.R. Bard Inc., manufacturers of vaginal mesh implants, to study rates of side effects such as organ damage, infection and painful sexual intercourse, which have been linked to the transvaginal mesh implants.* In addition to Johnson & Johnson and C.R. Bard, 31 oth
Contributor
About
PRWeb, a leader in online news and press release distribution, has been used by attorneys, law firms and more than 40,000 organizations
PRWeb, a leader in online news and press release distribution, has been used by attorneys, law firms and more than 40,000 organizations
Related Documents in PR Web
- Treatment for Jared Loughner Likely Was Doomed By New Public Policies, According To Book Released Th
- Gilman Law LLP is Investigating Claims Stemming From 'Off-Label' Use of Medtronic’s Infuse(R) Bone G
- The Consumer Justice Foundation Alerts the Public to the Consolidation of Federal Actos Bladder Canc
Categories
- Articles 308
- Bankruptcy 44
- Business 133
- Cases & Codes 68
- Contracts 27
- Criminal Law 122
- Employment 24
- Expert Reports 3
- Expert Witness 34
- Family Law 57
- Form Letters 15
- Immigration 3
- Intellectual Prop 32
- Internet Law 10
- Law Practice 99
- Law School 2
- Legal Research 19
- Litigation 186
- Miscellaneous 64
- PR Web 41689
- Personal Injury 608
- Press Release 43
- Probate 54
- Real Estate 68
- Tax Law 23
- Workers Comp 4