Stryker and DePuy Recalls

July 4, 2012- Stryker Rejuvenate and ABG II Following a safety notice to surgeons in the spring of 2012, Stryker announced it was recalling both the Rejuvenate and ABG II modular stem devices. The stems have the potential to corrode and/or "fret," creating the potential for metallic debris or ions that affect local tissue. August 24, 2010- DePuy ASR XL Johnson & Johnson, a parent company of DePuy Orthopaedics, recalled the DePuy ASR XL and ASR Resurfacing system after receiving new data showing that nearly 1 out of 8 hip replacements need to be redone. Approximately 93,000 people around the world have received one of the faulty DePuy hip implants.
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GoldenbergLaw, PLLC, is a national products liability and personal injury law firm located in Minneapolis, Minnesota. Our attorneys have successfully handled defective device and drug cases for over 27 years throughout the nation. We have obtained many millions of dollars in settlements for dangerous and defective drugs, products and devices. Manufacturers have a duty to create products that are safe when used in a way that the manufacturer should have foreseen.

GoldenbergLaw holds these companies responsible for actions that harm your health and well-being.

Defective medical devices can affect thousands of people nationwide. We have the desire, experience and resources to hold these companies responsible. Please visit our website for more information on our firm.

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