Knee Implant Recall: Smith and Nephew

Knee Implant: Smith & Nephew Recall *

Several Knee implants made by the medical device manufacturer Smith and Nephew have been recalled. In August 2003, Smith and Nephew recalled two models of Knee replacements and told the FDA of the problems associated with them.

The products included: cement less versions of Smith and Nephew: Oxinium Genesis II and Oxinium Profix II knee replacement systems. The company reported that corrective revision surgery was needed for about 30 of the 3,000 patients fitted with the products in the United States. However, many other patients may also need to be checked to make sure the Knee implant is not defective.

Patients who have these implants should contact us to get a free evaluation of their rights to both medical treatment and a compensation package for pain and suffering. Claims against manufacturer are being pursued on behalf of patients who have undergone unnecessary and painful revision surgery.

If you or a loved one has suffered from complications related to a Knee Implant, please fill out the requested information below. The information you submit will be kept private and confidential and used for the sole purpose of evaluating your case.

By submitting the form below you have read and agree to our terms and conditions.


First Name:

  M. I.


 Last Name:




 Zip Code:

 Phone Number (day):

 Phone Number (eve):

Email Address 

 If this inquiry is not for yourself, please tell us the name of the person?:



First Name:



Last Name:

What is the Injured's relationship to you?:

 Injured's Date of Birth:
ie (mm/dd/19yy)

Did you have knee replacement surgery? 

Who was the manufacturer of the knee replacement?:

 Date of Surgery?

Name of hospital where surgery was performed? 

City and state of where surgery was performed? 

 Name of doctor who performed surgery?

 Address of doctor who performed surgery (if known)?

 What adverse reactions did you have related to the surgery?

 Did adverse reactions make another Knee replacement necessary?

If yes, date of additional surgery?

If yes, what adverse reactions did you have related to the surgery? 

Please provide a brief description of what happened:
 I understand that submitting this form does not create an attorney client relationship: Agree

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