On July 4, 2012, Stryker posted on its website a national recall of its Rejuvenate and ADM hip implant systems. It’s obvious that Stryker has received far too many reports of shockingly premature failures of its hip implant. The Rejuvenate has only been on the market since 2009 so enough […]
Category: Defective Medical Devices
It is estimated that about 500,000 patients have received metal-on-metal hips, though firm numbers are hard to come by because the U.S. does not track medical device implants. In fact, that mystery is just one of many that surfaced on June 27 and 28, when the Food and Drug Administration (FDA) convened […]
(It Doesn’t Really Matter As Long As Patients and Surgeons Stop Buying the Defective Implants!) While it would certainly be nice to have a government that moved swiftly to recall defective drugs and medical devices from the market, we do not live in that world – at least in the […]
The Searcy Denney Mass Tort Unit would like to thank our client, Howard Sadwin of Sarasota, Florida, for his poignant statements today before the Orthopaedic and Rehabilitation Devices Panel of the Medical Devices Advisory Committee for the Food and Drug Administration. The hearings were convened in Gaithersburg, Maryland. In addition […]
As a Stryker hip implant attorney, I have written previously about our experience with clients who had Stryker hip replacement problems. Most of these clients tell us about conversations with their doctors before surgery in which they were told the Rejuvenate hip was better for them due to their young […]
The Searcy Denney Mass Tort Unit filed yet another individual lawsuit this week on behalf of a Florida DePuy ASR hip implant victim. This claim was filed on behalf of a Sebring resident who was implanted with bilateral recalled DePuy ASR implants in 2007 at Highlands Regional Medical Center. This plaintiff […]
It seems sort of nonsensical to blame the victim for his or her condition but that is what medical device maker Stryker appears to be doing in an April Field Safety Notice (FSN). In the United Kingdom, medical device manufacturers are required to report to the MHRA, their version of our […]
With all of the controversy, bad outcomes, and thousands of personal injury lawsuits concerning vaginal mesh, this medical doctor has a novel approach. Dr. John Wei of the University of Michigan suggests using a mid-urethral sling to prevent incontinence, even when the woman is not incontinent! Published June 20, 2012 […]
What do we know about any of the polypropylene meshes that are being removed from the market by Johnson & Johnson’s Ethicon division. The four involved mesh products are: The TVT Secur; The Prosima Pelvic Floor Repair System; The Prolift Pelvic Floor Repair System; and The Prolift MTM Pelvic Floor […]
Late last night, June 4th comes news from Bloomberg, that medical device maker, Johnson & Johnson (J&J) plans to stop selling four transvaginal mesh implants in the face of hundreds of lawsuits and more to come. Ethicon, a unit of J&J, told a federal judge in West Virginia that it […]
