Carrollton Zimmer Persona Recall Lawyer

The Parian Law Firm, LLC was among the first to learn of a voluntary recall by Zimmer, Inc. of all lots and sizes of the tibial component of the Zimmer Persona Trabecular Metal Knee System. The United States Food & Drug Administration (“FDA”) has now issued a Class II recall of the device due to an increase in complaints about the defective medical device loosening or having radiolucent lines post-surgery. This is yet another set back for manufacturers of joint replacement devices. According to the FDA Zimmer Persona recall notice, all affected products are to be located and quarantined immediately. Contact a product liability lawyer if you have been affected by a defective Zimmer Persona device. Our Carrollton Zimmer hip replacement recall attorneys are standing by and ready to assist.

Prevalence of Zimmer Knee Replacements

Remarkably, Zimmer brings in over $2 billion dollars per year on just knee replacements. As one can imagine, the orthopedic medical device market is competitive; therefore, manufacturers come out with “the latest and greatest” devices constantly. The Zimmer Persona Knee is the latest from Zimmer’s stable of knee replacement products. Although the risk of death due to the recalled tibial knee device is rare, it is not something to be taken lightly. You should contact your orthopedic surgeon to determine if you have one of the recalled knee devices.

Contact a Zimmer Knee Recall Lawyer

Our Carrollton Zimmer Persona Recall lawyers have been at the forefront of this Zimmer Knee Recall. We are currently assisting people throughout the United States with obtaining help with the defective device, as well as other defective medical devices. Contact us today.