The DePuy ASR Hip versus the DePuy Pinnacle Hip: What Are the Differences?

While the primary difference between the DePuy ASR hip implant and the DePuy Pinnacle hip implant lies in the fact that the ASR was recalled on August 26, 2010, there are significant design differences between the two implants. Both implants have labored under adverse reports from recipients.
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FDA Communications on Urogynecologic Mesh

This article will address the communications from the FDA regarding Urogynecologic mesh when used transvaginally in the correction of pelvic organ prolapse. The FDA issued the first Public Health Notification regarding this device in 2008, then in 2011 issued an update on the safety and effectiveness of transvaginal mesh used in repair of pelvic organ prolapse.
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Effectiveness of the FDA’s Warnings on Urogynecologic Mesh

This article will discuss the effectiveness of warnings issued by the FDA regarding the surgical use of urogynecologic mesh. Since the FDA first sent out a Public Safety Notification regarding mesh used in transvaginal pelvic organ prolapse surgery, they have been trying to get the word out to consumers and physicians about the potential risks involved.
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An Overview of the FDA Warnings on Urogynecologic Mesh

This article describes the FDA warnings associated with urogynecologic mesh as used in pelvic organ prolapse transvaginal surgical applications, as based on a recently published Current Urology Reports study,
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What is the Real Problem with the Stryker Rejuvenate Hip?

Although Stryker Orthopedics recalled their Rejuvenate hip implant this past July—ostensibly due to the potential of fretting and corrosion—there may be a different reason why this particular hip implant can be risky for recipients. At the end of June, 2012, an FDA panel of orthopedic surgeons convened to discuss whether there was any reason at all to continue using metal-on-metal hip implants.
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