Defective Medical Devices

DePuy Pinnacle Ultamet Hip Implants are similar to the DePuy ASR because both are metal-on-metal implants. There have been a large number of complaints about the DePuy Pinnacle Hip Implant including: hip pain, loosening, metal fragments and a need for additional revision surgery

.

DePuy ASR Hip Implants have been withdrawn from the U.S. market due to numerous reports of high failure rates in some patients which may lead to other injuries, excessive pain and the need for additional replacement surgery.

The FDA has recently warned about Transvaginal Mesh Implant complications and side effects. If you have been injured you may be entitled to compensation.

Wright Medical Conserve Plus & Profemur Hip Implants have had numerous reports of high failure rates in some patients. This may lead to other injuries, excessive pain and the need for revision surgery.

Defective Smith & Nephew Knee Replacement Recall. A recall has been issued for Smith & Nephew Oxinium Genesis II & Profix II Knee Implants due to possible defects that may higher than normal risk of injury to patients.

Defective Stryker Hip Implant Recall Lawsuit. If you have needed revision surgery or experienced problems with your Stryker Hip Implant you may be entitled to compensation.

Sales of defective Zimmer Durom Cup Hip Replacements have been suspended due to complaints of failure and crippling pain. Revision surgery may be needed in some patients to correct the problem.

Zimmer NexGen Knee Implants may fail early due to a design flaw which may cause it to losen, cause pain and may require revision surgery.

Transvaginal Mesh Implant Lawsuit. The Bard Avaulta Plus Biosynthetic Support System has been recalled due to side effects resulting from the implant.

The Gynecare Prolift Pelvic Floor System, like many other popular brands of vaginal mesh, has recently been linked to several complications.

The FDA has cited a serious and potentially life threatening design flaw in the Medtronic SynchroMed II Pain Infusion Pump and has issued a recall.

CooperVision’s AVAIRA Toric Soft Contact Lenses Recall issued due to an unintended presence of silicone oil residue, which can cause hazy or blurry vision, discomfort to the eye and injuries requiring medical treatment.

The Medtronic Infuse Bone Graft has been linked to serious and potentially life threatening complications when used in surgeries of the cervical spine, around the neck.