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DePuy Knee Sleeve Lawsuits Help: Resource4thePeople Expands Recall Reviews to include both Knee and Hip Cases
Date:9/6/2013

uy knee sleeves.

Class I recalls such as those issued for the DePuy knee sleeve and hip implant systems are the most serious type of recall and involve situations in which there is a reasonable probability that use of these products will cause serious adverse health consequences or death, the FDA said.

Among the DePuy knee sleeve problems being investigated are:

  •     Infections
  •     Pain
  •     Possible loss of limb
  •     Decreased range of motion
  •     Lengthening or shortening of leg
  •     Dislocations
  •     Subluxation
  •     Flexion contracture
  •     Bone fractures
  •     Shifts in the positioning of the device
  •     Loosening, bending, cracking, fracture, deformation or wear of one or more of the components

Resource4thePeople also is announcing the success of its new information center for consumers who are interested in allegations involving serious health problems linked to the recalls.

Among the features of the new information center is a link to a toll-free number through which consumers may seek the complimentary consultations being offered by the nationwide network of experienced attorneys familiar with the concerns raised by the FDA.

"There have been a substantial number of inquiries about allegations involving the DePuy knee sleeve in just the few weeks since the center was established," said Resource4thePeople.

Included in the information center are details of the FDA's recall announcement and details of some of the serious health problems that are now being investigated by Resource4thePeople attorneys.

FDA officials, in their “Reason fo
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