FDA Announces Stryker Spinal Plate Recall
The U.S. Food and Drug Administration (FDA) has announced the recall of the Stryker Spine OASYS Midline Occiput Plate over a potentially dangerous side effect, signaling that there is a “reasonable...
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Number of Medical Device Recalls Jumps 97 Percent From 2003 to 2012
According to the Minneapolis Star Tribune, the U.S. Food and Drug Administration (FDA) has revealed that the number of medical device recalls nationally doubled between 2003 and 2012. The paper...
View ArticleFourteen Plaintiffs File Suit against Stryker / Howmedica over CerviCore Implant
On Friday April 11, the law firm of Zoll, Kranz & Borgess, LLC filed a lawsuit on behalf of a group of fourteen plaintiffs against Howmedica Osteonics Corp. (which does business as Stryker Spine)...
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Medtronic to Settle Infuse Claims, Expected to Set Aside Funds for Future...
According to the Wall Street Journal, Medtronic said that it would pay $22 million to settle current claims over its controversial spine surgery product Infuse, and is setting aside $140 million for...
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