Joint replacements are the #1 expenditure of Medicare. The process of approving these medical devices is flawed according to the Institute of Medicine. It is time for patients' voices to be heard as stakeholders and for public support for increased medical device industry accountability and heightened protections for patients. Post-market registry. Product warranty. Patient/consumer stakeholder equity. Rescind industry pre-emptions/entitlements. All clinical trials must report all data.
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Monday, April 29, 2013

Bad Ad: Johnson & Johnson tarnished halo selling new 'product': love!

Have the FDA and FCC approved this ad?  
What product is this corporation selling?
Does it have to disclose that it is being sued by thousands of harmed patients?
(Metal on metal hips and surgical mesh.)


This bad ad will be aired:



History does not match JNJ we have today:

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