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Hip Replacement Recalls

During a hip replacement, a prosthesis or artificial part is surgically implanted into a person’s body to replace an injured or damaged joint. The goal of this procedure is to restore hip function, improve mobility, and ease pain. Unfortunately, the hip replacement sometimes fails because the device itself is defective. Recently, several hip replacement devices have been proven defective and been recalled.

Recalled Models

· Stryker® Rejuvenate and ABGII- Implanted between 2/2009- 7/2012.

· Stryker® LFIT v40 CoCr head with Accolade, Meridian and Citation TMZF stems implanted from 2001- present

· DePuy ASR Implanted between 2006- 8/2010.

· DePuy Pinnacle

· Zimmer Durom Cup

· Wright- Profemur, Conserve, Conserve Plus, Lineage, Dynasty

· Biomet- M2a 38

Stryker® is a registered trademark of Stryker Corporation. LFIT™and V40™are trademarks of Stryker Corporation. This law firm is not associated with, sponsored by, or affiliated with Stryker Corporation.

Side Effects of Defective Devices

· Metal poisoning (metallosis)

· Necrosis of surrounding tissue

· Hip stem breakage

· Implant dislocation

· Difficulty standing or balancing

· Bone fractures

· Joint noise

· Inflammation near implant site

· Severe pain

You May Be Entitled to Compensation

If you or someone you know received a recalled hip implant and suffered painful swelling or related side effects that resulted in hospitalization or a revision surgery, contact Lundy Law. We can help you get the compensation you deserve for your hip replacement injury. Fill out a free online consultation form or call us at 1-800 Lundy Law today.

Cases may be referred to associated law firms.

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