Search for: "ETHICON INC"
Results 181 - 200
of 288
Sort by Relevance
|
Sort by Date
3 Sep 2012, 9:21 am
Bard; Ethicon; Boston Scientific, American Medical Systems, Inc. [read post]
10 Aug 2012, 7:27 am
Bard, Avaulta, Boston Scientific, and Johnson & Johnson’s Ethicon. [read post]
9 Aug 2012, 5:00 am
Carter Wallace (pregnancy test) Deposition1998-12-22 Ethicon, Inc. v. [read post]
4 Aug 2012, 5:08 am
Bard, Avaulta, Boston Scientific, and Johnson & Johnson’s Ethicon. [read post]
1 Aug 2012, 5:39 pm
A New Jersey Superior Court Judge presiding over pelvic mesh litigation against Johnson & Johnson and its subsidiary Ethicon, Inc., has ordered three of the company [read post]
25 Jul 2012, 5:56 pm
Bard Inc. must pay $5.5 million in damages involving a vaginal-mesh implant that left a woman incontinent and in chronic pain. [read post]
25 Jul 2012, 5:56 pm
Bard Inc. must pay $5.5 million in damages involving a vaginal-mesh implant that left a woman incontinent and in chronic pain. [read post]
25 Jul 2012, 7:36 am
This includes the Gynecare TVT Secur system, Gynecare Prosima, Gynecare Prolift and Gynecare Prolift + M, all made by J&J subsidiary Ethicon. [read post]
24 Jul 2012, 9:36 pm
Bard, Inc.: Sold under the names Avaulta, Pelvisoft BioMesh, Pelivicol Acellular Collagen Matrix, Pelvitext, and Pelvilace Johnson & Johnson/Ethicon: Sold under the names Gynecare, Gynemesh, Gynecare Prolift, Gynecare Prolift+M, Gynecare Prosima and Gynecare TVT [read post]
24 Jul 2012, 9:36 pm
Bard, Inc.: Sold under the names Avaulta, Pelvisoft BioMesh, Pelivicol Acellular Collagen Matrix, Pelvitext, and Pelvilace Johnson & Johnson/Ethicon: Sold under the names Gynecare, Gynemesh, Gynecare Prolift, Gynecare Prolift+M, Gynecare Prosima and Gynecare TVT [read post]
29 Jun 2012, 1:19 pm
Currently, Ethicon Inc. and J&J are defending more than 1,400 transvaginal mesh implant lawsuits in both state and federal courts filed by individuals alleging that the Ethicon pelvic mesh implant systems caused them to develop vaginal mesh problems resulting in serious injuries. [read post]
25 Jun 2012, 2:01 pm
MDL No. 2381 - Intuitive Surgical, Inc., d/b/a Da Vinci Robotic Surgical System Products - Plaintiffs have requested centralization of the products liability litigation (which involves only 4 cases) in the Southern District of Mississippi or Northern District of California. [read post]
25 Jun 2012, 2:01 pm
MDL No. 2381 - Intuitive Surgical, Inc., d/b/a Da Vinci Robotic Surgical System Products - Plaintiffs have requested centralization of the products liability litigation (which involves only 4 cases) in the Southern District of Mississippi or Northern District of California. [read post]
25 Jun 2012, 2:01 pm
MDL No. 2381 - Intuitive Surgical, Inc., d/b/a Da Vinci Robotic Surgical System Products - Plaintiffs have requested centralization of the products liability litigation (which involves only 4 cases) in the Southern District of Mississippi or Northern District of California. [read post]
13 Jun 2012, 12:00 am
Ethicon Inc., a wholly owned subsidiary of Johnson & Johnson, has decided to cease marketing and producing four types of vaginal mesh implants. [read post]
8 Jun 2012, 8:29 am
With ongoing litigation against Ethicon Inc., those who have experienced complications may be entitled to compensation. [read post]
7 Jun 2012, 12:37 pm
The defendants, Johnson & Johnson and Ethicon, Inc., designed, made, marketed, and sold pelvic mesh medical devices for the treatment of pelvic organ prolapse and stress urinary incontinence. [read post]
6 Jun 2012, 12:41 pm
Bard, Inc. [read post]
5 Jun 2012, 1:22 pm
Johnson & Johnson's subsidiary and pelvic mesh manufacturer, Ethicon, Inc., informed the FDA yesterday that it is recalling four of its Pelvic Floor Repair Systems and is asking for 120 days to “cease commercialization” of its products, notify customers and allow physicians and hospitals time to choose different treatments for patients. [read post]
5 Jun 2012, 1:22 pm
Johnson & Johnson's subsidiary and pelvic mesh manufacturer, Ethicon, Inc., informed the FDA yesterday that it is recalling four of its Pelvic Floor Repair Systems and is asking for 120 days to “cease commercialization” of its products, notify customers and allow physicians and hospitals time to choose different treatments for patients. [read post]
