DePuy Knee Replacement Recall

FDA Recalls DePuy Leg Joint Component Because of Fracture Risk

In Feb 2013, the FDA granted a Course I remember – used only once there is affordable probability a product may cause serious negative health outcomes or fatality – for the diaphysis sleeve found in Deputy’s leg LPS.

Based on the FDA, the joint part poses a fracture risk, which can result in serious difficulties for the receiver. If you are looking for depuy attune knee lawsuit, then you can check out this web link:

DePuy Knee Lawsuit | Attune Knee Failure Lawsuits

Specifically, the FDA declared that the taper interconnection between your sleeve and the bottom might not have the ability to withstand loads used in the joint during normal, everyday movement.

If the sleeve fractures at the taper joint, lack of function, lack of limb, contamination, compromised soft muscle or fatality may result.

DePuy Knee Replacing Problems

Signs of failing may include the next:

  • Limited selection of movement
  • Infection
  • Dislocation
  • Warm, swollen or red skin
  • Stiffness
  • Instability in the knee
  • Fracture
  • Loosening of the leg implant

Abnormal gait

On Jan. 4, 2012, the FDA knowledgeable hospitals and doctors of the actual problem with the sleeve and asked them to avoid using the recalled plenty.

Based on the FDA, all diaphysis sleeves made between 2008 and July 2012 is damaged by the recall. As of yet, the FDA has received 10 reviews of device breakdown, specifically related to fracture and loosening of the leg implant.

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