Comments on: Johnson & Johnson hit with FDA warning letter | MassDevice – Medical Device Industry News

By: FDA Confirms Johnson & Johnson Prolift Pelvic Mesh Product Sold for Over 3 Years without Necessary FDA Clearance « Earl's View

Fri, 23 Mar 2012 23:25:16 +0000

[...] Johnson & Johnson hit with FDA warning letter | MassDevice – Medical Device Industry News (earlsview.com) [...]

By: FDA Workers Say Outsiders Influence Medical Device Decisions | Patrick Malone & Associates P.C. | DC Injury Lawyers – JDSupra « Earl's View

Fri, 23 Mar 2012 23:16:41 +0000

[...] Johnson & Johnson hit with FDA warning letter | MassDevice – Medical Device Industry News (earlsview.com) [...]

By: Gynecare Prolift Mesh Sold by J&J Without FDA Approval | InjuryBoard Fort Worth « Earl's View

Fri, 23 Mar 2012 23:10:25 +0000

[...] Johnson & Johnson hit with FDA warning letter | MassDevice – Medical Device Industry News (earlsview.com) [...]

By: Consumer Reports taps ire over bad medical devices « Earl's View

Consumer Reports taps ire over bad medical devices « Earl's View — Tue, 13 Mar 2012 19:51:33 +0000

[...] Johnson & Johnson hit with FDA warning letter | MassDevice – Medical Device Industry News (earlsview.com) [...]

By: Earl's View

Earl's View — Thu, 16 Feb 2012 12:02:05 +0000

[...] Johnson & Johnson hit with FDA warning letter | MassDevice – Medical Device Industry News (earlsview.com) [...]

By: Johnson & Johnson Takes $3 Billion Charge for Hip Recall – NYTimes.com « Earl's View

Wed, 25 Jan 2012 09:39:53 +0000

[...] Johnson & Johnson hit with FDA warning letter | MassDevice – Medical Device Industry News (earlsview.com) [...]

By: FDA warns J&J’s DePuy unit over joint replacements – AlertNet « Earl's View

Thu, 19 Jan 2012 11:52:32 +0000

[...] Johnson & Johnson hit with FDA warning letter | MassDevice – Medical Device Industry News (earlsview.com) [...]

By: earlstevens58

earlstevens58 — Sat, 14 Jan 2012 23:44:14 +0000

Absolutely right!

Earl

By: Howard Sadwin

Howard Sadwin — Sat, 14 Jan 2012 18:42:48 +0000

This is a reflection of the incompetent way in which the FDA handles such matters, or maybe I should say the competent way the medical device world does handle the matter. For the life of me, if there is enough apparent problems with a medical device take it off the market, put it on the shelf and correct the problem.
This demonstrates the importance of Market Share, Finances and don’t forget the Investors, sell, sell, sell, so what if a few people get hurt.
The FDA sends a warning letter and then what do they do ? Send another warning letter or slap on the medical device manufacturers wrist, mean while innocent people are getting hurt. Is this justice or is this just another way for the FDA to demonstrate its weakness when dealing with the medical device world. This isn’t about the lack of funds to employ people to enforce the law, this is just another poor example of who is running the show, the medical device world.
Respectfully
Howard Sadwin