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Dozens of defective hernia mesh medical devices have been recalled. Some were recalled by the Food and Drug Administration (FDA), although most were voluntarily recalled by the hernia mesh manufacturers after several patients reported injuries from having hernia mesh.
2 Φεβ 2024 · JPMorgan Chase & Co. C.R. Bard Inc. and Davol Inc. were granted summary judgment on several tort claims concerning the 3DMax hernia mesh device in a bellwether trial that’s part of a multidistrict litigation involving thousands of cases.
5 Σεπ 2020 · Starting in 2005, C.R. Bard subsidiary, Davol, initiated a large-scale recall of its Composix Kugel mesh patch line following increasing reports of complications and painful revision surgeries in patients where it was used.
2 Οκτ 2024 · The MDL centralized claims regarding alleged injuries caused by Bard’s hernia mesh products, simplifying pre-trial proceedings for the tens of thousands of federal cases filed.
18 Οκτ 2024 · The mesh lawsuits, some of which go back almost 20 years, allege that Bard designed defective mesh products, failed to adequately test them, and didn’t properly warn users about potential risks.
5 Μαΐ 2017 · Thousands of mesh victims filed Bard hernia mesh lawsuits against Bard and their corporate subsidiary, Davol, seeking compensation by way of settlements or legal judgment as a result of purported defective hernia mesh and hernia patches.
3 Οκτ 2024 · Levin Papantonio law firm has announced the establishment of a global resolution process for the third largest multidistrict litigation (MDL) in the U.S.—MDL 2846 IN RE: Davol, Inc./C.R. Bard, Inc., Polypropylene Hernia Mesh Products Liability Litigation.
