DePUY HIP IMPLANT

RECALL

Much like Stryker Corporation’s Rejuvenate and ABG II metal hip implants, hip implant devices manufactured by DePuy have also been recalled from the market after causing serious harm in thousands of patients. In 2010, the FDA issued a worldwide recall of the DePuy ASR 300 Acetabular Cup System.

This metal hip implant device was implanted in an estimated 93,000 patients worldwide prior to the recall.

In 2013, DePuy and its parent company Johnson & Johnson announced a major settlement agreement related to the ASR hip implant system. The companies set aside $2.5 billion to settle approximately 8,000 individual lawsuits brought by injured patients, that required revision surgery after receiving a DePuy ASR metal hip implant device.

In 2015, DePuy and Johnson & Johnson announced a second settlement agreement worth $420 million with patients that were not included in the original 2013 agreement.


Fellows Hymowitz Can Help

At Fellows Hymowitz, our experienced Defective Medical Device Attorneys fight hard to hold manufacturers responsible for the pain and suffering their defective products can cause. Call us today at 845-639-9300 for a FREE, confidential consultation.

When you contact Fellows Hymowitz, one of our caring, dedicated attorneys will investigate every detail of your situation at no cost to you. We will help you find answers and fight hard to protect your rights. Also, you will never pay an attorney’s fee up front, and you owe us nothing unless we recover for you. Call us today to learn how we may be able to help.

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