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Have You Been Affected by the Stryker Hip Recall?
Stryker, a Michigan-based corporation, issued a Stryker hip recall in July, 2012, on the heels of an urgent field safety notification which went out to hospitals and surgeons just three months’ prior. Both the safety notification and the recall notice stated the Rejuvenate and ABGII had a higher-than-normal rate of failure due to excess fretting and corrosion. This fretting and corrosion could then lead to the release of cobalt and chromium ions into surrounding tissue and into the bloodstream. This came as a surprise to many as Stryker aggressively marketed the new hip implants as much safer than a “true” metal-on-metal hip implant due to the use of a ceramic ball rather than a metal ball. Unfortunately, the neck/stem junction was later found to create ion debris during periods of patient activity.
The small metal trunnions located on either end of the neck component were also found to release metal ions when body fluids became trapped underneath. Over 20,000 patients received a Rejuvenate or ABGII between February 2010, when both models were released (after FDA approval in 2008 and 2009) and the time the recall was issued. Within a few short months of the release of the two Stryker hip implants, adverse reports were being sent to the FDA. Some surgeons who were forced to remove one of these implants from a patient noted the presence of a substance which looked like “black rust.” Others noted a white, milky substance in the hip tissues. By early 2012, over 300 adverse reports had come into the FDA, yet Stryker continued to sell the devices until the recall. Perhaps you, like many others have reason to file a Maryland Stryker hip lawsuit. If so, it is very important that you speak to a Maryland Stryker hip lawyer as soon as possible to avoid exceeding your state’s statute of limitations.
Health Problems Associated With the Stryker Hip Recall
The metal ions in the hip tissues were found to cause destruction and death of bone and tissue, total hip failure, acute inflammation, chronic pain in the groin, leg and thigh and the necessity of revision surgery. Cobalt and chromium ions in the bloodstream can lead to a variety of serious health issues such as:
· Gastrointestinal, renal, thyroid, cardiovascular and neurological disorders
· Loss of hearing or vision
· Anxiety, depression, irritability
· Vertigo and memory loss
· Reproductive disorders
· DNA changes
· The development of pseudo-tumors
How the Maryland Stryker Hip Statute of Limitations May Affect You
All states have a specific statute of limitations which allows consumers a specific length of time in which to file a lawsuit against the manufacturer of a defective product. In the state of Maryland, action must be brought within three years of the date the injury occurred. In the case of the Stryker hip recall, determining the exact date can be complex. Perhaps you realized you were sick, but did not realize your symptoms were related to your defective Stryker hip device. Or perhaps you have not yet suffered any adverse health symptoms, but are wondering how to protect your rights in the event you do develop symptoms associated with the Stryker hip recall. The best way to get trustworthy information regarding your right to file a Maryland Stryker hip lawsuit and to ensure the statutes are not exceeded is to speak to a knowledgeable Maryland Stryker hip lawyer. You may have medical expenses related to your defective Stryker hip implant, therefore the Maryland Stryker hip statute of limitations is extremely important. Don’t miss the window of opportunity for filing a Maryland Stryker hip lawsuit—call a Stryker attorney today to get the information you need for your future.