Here’s an update on the court case currently underway in the U.S. which may prove a bellwether for future proceedings … continue reading “Kransky vs J&J DePuy Trial Closing Remarks”
Johnson & Johnson
$3.35M Award For Nurse In J&J Vaginal Mesh Case
J&J should pay a South Dakota nurse $3.35 million according to the jury in the much-reported vaginal mesh trial. They found that the company had failed to provide adequate warning of risks to the plaintiff’s doctor. J&J’s rebuttal to follow.
Kransky vs DePuy: Chromium Didn’t Poison Patient Says Toxicologist
So did chromium from wear particles in DePuy’s ASR hip system poison Mr Kransky? A prominent toxicologist says no, but then his work is undermined by the plaintiff’s attorney who implies bias. It’s feisty stuff.
J&J’s Ethicon Unit Faces Uphill Battle In New Jersey Transvaginal Mesh Trial, Says Legal-Bay LLC
The Lawsuit Settlement Funding Company, which has been a public advocate for women victims of various vaginal and pelvic mesh implants, reported today that industry insiders close to the Ethicon Prolift mesh trial have advised them that the plaintiff’s case has raised serious concerns as to what J&J knew about the dangers of their mesh products.
DePuy “did more testing on the ASR than any other product we put on the market”
Update on proceedings between “vasculopath” Loren Kransky and J&J (DePuy), centring on whether the company poisoned the plaintiff.
FDA Nod For Ethicon Endo’s ENSEAL® G2 Articulating Tissue Sealer
Ethicon Endo-Surgery says its ENSEAL® advanced bipolar devices are strong on sealing, yet gentle on tissue. And now with a new Articulating iteration these benefits can be exploited in the most difficult-to-access anatomies.
12%, 37% or 49%? What Exactly Is DePuy’s All-Metal Hip Failure Rate At 5 Years
Bloomberg has reported on the pre-trial testimony of Paul Voorhorst, a DePuy biostatistician, as a preamble to proceedings in the case of Loren Kransky vs J&J (DePuy), for which the jury sits tomorrow (Friday 25th January). In it, previously unseen documents suggest that the company’s own estimates of failure rate for some of its metal-on-metal hip prostheses are now as high as 37%, significantly higher than the 12 or 13% cited in the original recall notices.
J&J Spells Out Growth Strategies
Today sees J&J’s annual business review at which the company says it will lay out its strategic ideas for growth. Its press release offers few surprises and could be summarised as “more of the same”, which is no bad thing looking at the financial results for 2012.
Class I Recall For Ethicon’s SurgiFlo Due To Potential for Packaging Breach
Ethicon, a division of J&J, has identified an issue in the packaging process for its SurgiFlo haemostatic matrix. It seems certain products, manufactured between September 16 2011 and July 27 2012 are susceptible to a potential breach of the double Tyvek pouch of the packaging.
Depuy Synthes Spine Unveils New Worldwide President
Johnson & Johnson’s DePuy Synthes Spine business has a new Worldwide president in the form of Max Reinhardt, a long term employee of the company and most recently Vice President of Worldwide Marketing.
FDA Approves EVARREST™ Fibrin Sealant Patch
Ethicon Biosurgery, has announced that the U.S. Food and Drug Administration (FDA) has approved EVARREST™ Fibrin Sealant Patch, a novel product that it says rapidly and reliably aids in stopping problematic bleeding during surgery.
Cordis Incraft™ AAA Stent Graft Promising 1 Year Clinicals
J&J subsidiary, Cordis has seen its Incraft AAA stent graft study results reach 1 year with no problems and 100% efficacy. The graft, with its 13Fr delivery system aims to extend EVAR To More Patients than currently indicated.
New Approval Means Cordis Has First Stent In The U.S. With SFA And Iliac Indications
J&J subsidiary, Cordis Corporation has announced that the U.S. FDA has approved its S.M.A.R.T.® CONTROL® Vascular Stent Systems for use in the superficial femoral artery and/or the proximal popliteal artery.
FDA Class I Recall For Bum Guns
Ethicon endo’s voluntary recall of certain Proximate Circular staplers during the summer has turned in to an FDA Class I recall due to the serious consequences that can befall the patient in whom the stapler has not completely fired.
Johnson & Johnson Reports 2012 Third-Quarter Results:
J&J’s sales of $17.1Bn for the third quarter of 2012, represent an increase of 6.5% compared to Q3 2011. Synthes product sales contributed 5.8% to worldwide operational sales growth, net of the divestiture of the DePuy trauma business.
No More “Just Put Your Finger On This” As Ethicon Launches What It Calls A “Knotless Tissue Control Device”
J&J division Ethicon, Inc., has followed Covidien into the barbed suture market with the launch of its new portfolio of Stratafix™ Knotless Tissue Control Devices. The idea is that barbed sutures offer significantly more points of fixation than traditional sutures, giving surgeons more consistent control over every pass (through the tissue), and combining the strength and security of interrupted closure with the efficiency of continuous closure.