Increased Metal Levels from Stryker Hip Implants: Cobalt Metal Poisoning from Recalled Stryker Rejuvenate & ABGII Hips

Patients with Stryker ABGII or Rejuvenate hip implants could see a wide variance between the cobalt and chromium levels with the cobalt levels being considerably more elevated. The probable reason for the difference in these numbers is that the wear in the Rejuvenate and ABGII hip implants does not come from the cup and ball portion of the joint rather it comes from the stem and neck. The design of these Stryker devices implements a Morse taper between the stem and the neck.  The Morse taper is a slightly angular junction which the physician hammers into the stem until it is snug, then hammers again so it will lock tightly.

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The Differences between the Recalled DePuy ASR and the DePuy Pinnacle Hip Implant: Is Your Hip a Recalled Version?

If you are the recipient of a DePuy hip implant device it is very important that you know which brand you were implanted with so you can be aware of the individual characteristics. Of course the primary difference between the ASR and its successor, the Pinnacle, is that the ASR was recalled in August, 2010, while the Pinnacle has not been recalled.
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How Do You Prove Your Transvaginal Mesh is Failing?

Knowing how transvaginal mesh is constructed can help women implanted with the mesh to understand how it can potentially fail and how that failure can be documented.
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Stryker Hip Recall: Measuring Stryker Rejuvenate Hip Failure Symptoms – ALVAL and Cobalt Elevated Levels

If ALVAL is suspected—usually when the patient suffers consistent groin pain which restricts their normal activities—tests for infection should be considered. Should there be an absence of infection yet the groin pain continues, revision to an implant made of a different substance may be recommended.
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How Dangerous is Your Transvaginal Mesh or Bladder Sling?

If you are a recipient of transvaginal mesh used in the repair of pelvic organ prolapse and have experienced significant health issues, you may wonder just how dangerous your mesh or bladder sling really is. Those women who have suffered significant mesh erosion, the formation of adhesions, extrusion, fistula formation, infection or sepsis, vaginal shortening, nerve injury or scar formation which results in mesh contraction may be forced to undergo revision surgery.

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