Search for: "Gynecare, Inc." Results 61 - 73 of 73
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7 May 2011, 7:16 pm by Ed Wallis
FREE CASE EVALUATION: CALL 1-800-632-1404 The DePuy hip recall of the ASR hip implant was announced by DePuy Orthopedics Inc. on August 26, 2010. [read post]
26 Feb 2011, 4:49 am by Ed Wallis
FREE CASE EVALUATION: CALL 1-800-632-1404 The DePuy hip recall of the ASR hip implant was announced by DePuy Orthopedics Inc. on August 26, 2010. [read post]
27 Dec 2010, 9:40 am by Ed Wallis
FREE CASE EVALUATION: CALL 1-800-632-1404 The DePuy hip recall of the ASR hip implant was announced by DePuy Orthopedics Inc. on August 26, 2010. [read post]
27 Dec 2010, 9:34 am by Ed Wallis
FREE CASE EVALUATION: CALL 1-800-632-1404 The DePuy hip recall of the ASR hip implant was announced by DePuy Orthopedics Inc. on August 26, 2010. [read post]
20 Dec 2010, 6:07 pm by Ed Wallis
FREE CASE EVALUATION: CALL 1-800-632-1404 The DePuy hip recall of the ASR hip implant was announced by DePuy Orthopedics Inc. on August 26, 2010. [read post]
24 Nov 2010, 4:28 am by Ed Wallis
One of Johnson & Johnson’s subsidiaries, DePuy Orthopedics, Inc, announced a recall of two kinds of hip implants this past Thursday. [read post]
9 Aug 2010, 7:59 pm by Ed Wallis
Hoffmann LaRoche Inc., ATL- L-8213-05, New Jersey Superior Court, Atlantic County (Atlantic City). [read post]
25 May 2010, 7:54 am by Ed Wallis
He also represents clients across the country pertaining to medical device failures, including the Advanced Bionics HiRes90k cochlear implant and the Gynecare Prolift transvaginal mesh – sling. [read post]
18 May 2010, 8:49 am by Ed Wallis
Free Case Evaluations Provided for Those Hurt and Injured by TVT Tape, Sling and Mesh Products Lawsuits have been filed, including in the Superior Court of New Jersey, for damages resulting from the Ethicon, Inc., Johnson and Johnson, and Gynecare Wordwide Transvaginal Mesh Sling. [read post]
20 Jan 2010, 12:38 pm by Beck, et al.
Ethicon, Inc., a wholly-owned subsidiary of Johnson & Johnson, manufactures a competing product, “Gynecare TVT. [read post]
6 Nov 2008, 11:50 am
The following chart contains the information that I have found: Manufacturer Product Name (Device) Number of MAUDE Events Date Range … [read post]
29 Oct 2008, 4:53 pm
SRI then informed the FDA that any differences between its device and the Gynecare equivalent did not raise new questions of safety and effectiveness. [read post]
26 Aug 2008, 10:18 am
The FDA has since requested that Davol, Inc. recall its Kugel Mesh Patch device. [read post]