DRUG/PRODUCT ALERT
Zimmer Hip Recall
Galfand Berger is investigating the complications caused by Zimmer hips. People who have used this product have suffered from:
Zimmer Holdings, the nation’s largest producer of orthopedic devices, has recalled its Durom cup, a hip socket, due to high failure rate. The medical device was first sold in the U.S. in 2006 and has been implanted in 12,000 patients.
WHAT SHOULD YOU DO?
If you, a family member or friend have used a Zimmer hip and experienced any unusual side effects, contact your doctor’s office or hospital about your injury.
In order to determine whether you have a right to be compensated for your injuries, please contact Galfand Berger at 1-877-228-1528.
