Stryker Hip Recall

Stryker hip recall
The Food and Drug Administration (FDA) regularly monitors all new drugs and medical treatment options which are entering the US market. They act as a quality assurance buffer to guarantee that the American people are provided with safe and effective products. Occasionally, the FDA issues recall notices advising companies and manufacturers to pull a product off the shelves because it may be hazardous to consumer health. The manufacturer must then conduct thorough testing and improve the quality of the drug before re-release into the market.

Hip replacement products are items which come under FDA scrutiny as well. Hip replacement surgery is often carried out in the elderly who develop problems with their hip bones and have trouble moving about. The thigh bone may be capped with a metallic ball for long-lasting effect, and part or the entire pelvis may also be replaced with metallic components to restore normal movement in the individual.

Stryker Corporation is a Michigan-based company which focuses on producing orthopedic products. Founded in 1941, the company has been steadily improving its stand in the global market and commands a higher share of the orthopedic market than its closest competitors. Since the 1990s, the corporation has also been acquiring several smaller orthopedic companies to expand its operations, further strengthening its position in the market. Recently though, a stryker hip recall was issued in light of evidence which pointed out the hazards of Stryker’s products.

Stryker hip recall – the case itself
Stryker Corporation voluntarily issued a recall on its hip replacement products last June after receiving information about the flaws in the product. The friction between the metallic components in the replacements was causing individuals to experience severe discomfort, limited flexibility, and even metal poisoning. In order to rectify these flaws and improve the quality of the product, the Stryker hip replacement recall was issued.

Several individuals across the United States have filed lawsuits against the company, claiming damages and costs of revision surgeries. The products in questions are Stryker’s Rejuvenate and ABG II Modular Neck Hip Stems. If you or someone you know underwent a procedure involving these products, you should consult an orthopedic surgeon immediately in order to determine the integrity of your hip components. Some individuals developed asymptomatic reactions as a result of the replacement surgery, and are eligible to receive compensation as well.

One of the reasons cited for the Stryker hip recall was the lack of thorough testing before the product was launched into the market. Because of its initial promise and the high demand for such a treatment, the products were fast-tracked without undergoing a rigorous vetting process. It was also granted approval by the FDA because of its resemblance to a previously approved product launched by another company. The consequences of the haste are now expected to cost Stryker Corporation up to $390 million.

This is not the first time that a Stryker hip recall has been issued. In 2007, the company issued a voluntary recall of another product called the Trident hip. If you or someone you know who has suffered on account of a faulty product, it may be worth your while consulting a personal injury lawyer specializing in product recall.

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Q:What is a Stryker hip replacement recall?

A:Stryker is a renowned manufacturer of medical devices and medical equipment. Many people suffering from hip join problems have undergone hip replacements. However, the product turned out to be faulty in many cases, causing victims to sue against the company. The company has advised many physicians about its faulty hip implants and the possibility of health complications.

Q:Can you tell what was the reason behind Stryker hip recalls?

A:Stryker has advised many physicians about the complications arising from its popular hip implants. Many people who have undergone hip replacements are taking legal action the manufacturer for medical issues caused by the device. These include high ion level in blood, psychological stress, pain and infection, depression and confusion, and heart complications.