Quantcast
Ennis & Ennis, P.A. | Personal Injury Attorney
1.800.856.6405

Follow Us

 

Defective Hip Implant Lawyer

____________________________________________________________________

Stryker Rejuvenate Hip Implant Lawsuit News Update
____________________________________________________________________

 



Bookmark and Share
 

Recall -- Firm Press Release

FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.

Stryker Initiates Voluntary Product Recall of Modular-Neck Stems
Action Specific to Rejuvenate and ABG II Modular-Neck Stems

- FDA

07/10/2012 - Stryker has voluntarily recalled its Rejuvenate and ABG II modular-neck stems.

"While modular-neck stems provide surgeons with an option to correct certain aspects of a patient’s anatomy and hip bio mechanics, given the potential risks associated with fretting and corrosion at the modular neck junction, Stryker decided to take this voluntary action," said Stuart Simpson, Vice President and General Manager, Hip Reconstruction.

Stryker Orthopaedics’ decision to voluntarily remove Rejuvenate and ABG II modular-neck stems and terminate global distribution of these products comes after continued post-market surveillance. The post-market surveillance data may be predictive of a trend. "Following this action, we will work with the medical community to better understand this matter as we continue to evaluate the data," said Simpson.

Stryker has notified healthcare professionals and regulatory bodies of this voluntary recall. Patients who received a Rejuvenate Modular or ABG II modular-neck stem are encouraged to contact their surgeon. Patients uncertain if they have one of these products implanted should contact their surgeon or consult their medical records.

A dedicated patient call center can be reached at 1-888-317-0200 and additional information can be found at www.AboutStryker.com/ModularNeckStems .

Defective Stryker Hip Implant Lawsuit::

If you or a loved one have been injured as a result of a defective metal on metal hip implant you may be entitled to compensation. Our experienced Stryker Rejuvenate Hip Replacement Attorneys are here to answer any questions you may have about a Stryker Rejuvenate or ABG II hip replacement lawsuit or a possible hip implant class action lawsuit. Fill out the free Stryker hip implant lawsuit case evaluation form on this page or contact our Hip Replacement Recall Lawsuit Lawyers directly by calling toll-free: 1.800.856.6405.

Offices:
Washington DC Office
1101 Pennsylvania Ave.
Suite 600
Washington, DC 20004
Telephone: 202.756.2972
Miami Office
1111 Brickell Avenue
11th Floor
Miami, FL 33131
Telephone: 305.913.7199
Fort Lauderdale Office
110 E. Broward Blvd.
Suite 1700
Fort Lauderdale, FL 33301
Telephone: 954.315.3934
Facsimile: 954.315.3914


Required fields in RED
 
Name:
Email:
 
Telephone: (123-123-1234)
 
Mailing Address:
 
City:
 
State:
 
Zip Code:
On whose behalf are you inquiring?
Is the person deceased?
Yes No
If the person is deceased please list the cause of death as listed on the death certificate:
 
Please list the date the device was implanted (MM/DD/YYYY):
 
Please describe any injuries that resulted from the implant as well as treatment received for the respective injuries:
 
Please list any additional information you feel may be relevant to your potential hip replacement case:
 
How did you hear about us?
 
1.800.856.6405
©2010 Ennis & Ennis, P.A. All rights reserved.