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Depuy Hip Replacement Helpline, Pennsylvania Depuy Hip Replacement Lawyers

DePuy Hip replacement Helpline Pennsylvania, DePuy Hip Recall Lawyers

Call the dePuy hip replacement Helpline Pennsylvania and speak to a medical social worker and DePuy Hip recall lawyer today. DePuy hip replacement Helpline Pennsylvania is hearing from people with the recalled ASR in Altoona, Cumberland valley, Erie, Harrisburg, Lancaster, Meadville, Philadelphia, Pittsburgh, Poconos, Reading, Scranton, State College, Williamsport, York, and all of Pennsylvania.

On August 26, 2010, DePuy announced the voluntary recall of the DePuy ASR Hip Replacement due to a high failure rate. The recall comes to late for the thousands of victims suffering from a failed hip Implant, Call the DePuy Hip Replacement Helpline and speak to a medical social worker and learn the facts about your failed DePuy. DePuy Hip Replacement helpline Lawyers are filing lawsuits for victims of the failed DePuy. Justice for the victims must be sought. A message must be sent to those who favor profits over people

The DePuy Hip Replacements Implants recalled are:

  • Depuy ASR XL Acetabular System
  • Depuy ASR Hip Resurfacing System

 Hip Implants that have been recalled other then the DePuy Hip Replacement are:

  • Zimmer Durom Cup
  • Stryker Rejuvenate Modular Hip System and ABG II modular-neck hip stems
  • Stryker Trident Hemispherical Acetubular Cup

Pennsylvania Zimmer NexGen Knee Replacement Helpline Lawsuit Division

The Zimmer Knee Replacement Helpline division will connect you with  a Zimmer NexGen Hip Replacement lawyer. Zimmer NexGen lawsuits have been  consolidated in multidistrict litigation (MDL) being held in the U.S. District Court for the Northern District of Illinois.

  • Zimmer NexGen “High-Flex” femoral components
  • Zimmer CR Flex
  • Zimmer Legacy Posterior Stabilized (Zimmer LPS Flex);
  •  Gender Solutions (Zimmer Gender Solutions High-Flex Knee)
  •  Zimmer MIS Tibial component (MIS Total Knee Procedure Stemmed Tibial Component Fixed Bearing Precoat)

NEW HIP REPLACEMENT RECALL NEWS

New Stryker Hip Replacement Recall, Metal Components Hip Replacement
Stryker Orthopaedics Recalls Rejuvenate Modular Hip System

New Stryker Hip Replacement Helpline and Stryker hip replacement lawyers offering help to people with a failed Stryker hip replacement

In July 2012, Stryker Orthopaedics voluntarily recalled its Rejuvenate Modular Hip System. The recall includes both Stryker’s Rejuvenate Modular and ABG II modular-neck hip stems.
Probelms include:

  •     Joint loosening and dislocation of the connecting joint
  •     corrosion and fretting of the device
  •     metal debris leading to metal  toxicity
  •     Inflammation of  surrounding tissue
  •     allergic response
  •     Broken devices in the hip after the surgery

The DePuy Hip Replacement Helpline lawyers are accepting clients and reviewing files for all failed hip implant victims.

Complications of a Failed DePuy Metal on Metal Hip Implant 

  • Pain in the groin, hip or leg
  • Swelling at or near the hip joint
  • A limp or change in walking ability
  • Continued pain
  • The need for a second surgery
  • The need for tests and medical monitoring on hip replacements that have yet to go bad
  • Costly medical bills
  • Loss of enjoyment of certain activities
  • Hip fracture
  • loosening of the Implant
  • swelling
  • Pain
  • Popping
  • Grinding
  • Metal sensitivity
  • Toxicity from the metal on metal rubbing
  • High levels of Chromium and Cobalt in the bloodstream with side effects from toxicity
  • Loosening of the prosthesis
  • infection
  • inability to walk
  • Dislocation where the two parts of the implant that move against each other are no longer aligned.
  • Fracture, where the bone around the implant may have broken
  • Severe limitations in daily activities and decline of quality of life
  • High metal ions levels in their bloodstreams
  • Loosening, when the implant does not stay attached to the bone in the right position

Lawsuits are Being Filed against the Manufacturers of the DePuy

DePuy Hip Replacement lawyers are filing lawsuits against hip replacement manufacturers DePuy Orthopaedics, Inc over failure of a DePuy ASR metal-on-metal hip replacement. The lawsuit against DePuy was filed in Federal District Court in Ft. Myers, Florida . This is believed to be the first lawsuit filed in the United States over the failure of the DePuy ASR hip replacement.

Call the DePuy Hip Replacement Helpline and speak to a Medical Social Worker about you faulty DePuy. DePuy Hip Replacement lawyers are accepting cases fro victims of failed DePuy Hip Replacements and Metal toxicity complications.

The Depuy Lawsuit

The DePuy lawsuit alleges that the DePuy ASR hip replacement was defectively designed. It claims DePuy knew that their ASR hip replacements were failing at a higher than expected rate, yet it did not pass that information on to consumers or orthopaedic surgeons. As a result, diagnosis that the ASR hip replacement implanted in the patient has failed was needlessly delayed as her physicians were unaware of the prevelance of other failures. During the patient’s surgery to replace the failed hip replacement, her orthopedic surgeon discovered that the cup portion of the ASR hip replacement was extremely loose. The ASR hip replacement is designed so that a patient’s bone grows into the back of the cup to secure it. However, loosening because of a lack of bone in-growth into the cup is a hallmark of DePuy ASR hip replacement failures.

 DePuy’s Recall comes too Late

Unfortunately, DePuy’s recall of the ASR systems comes too late for patients that were implanted with these devices. This is not a typical recall where the toy with lead paint can simply be discarded or returned to the manufacturer for a refund. This recall is for a product that has been implanted in a person’s hip. As a result, the recalled product can only be replaced with the patient going through a painful and debilitating surgery and rehabilitation. In addition there are concerns about toxicity from the metal components rubbing. Patients are advised to have their blood levels checked for Chromium and Cobalt levels.

 High Failure rate

Many observers expect this already high failure rate to increase dramatically as problems with the DePuy ASR hip systems become more widely publicized. Denying that its decision to do so was related to reports of failures of the ASR systems, late last year DePuy ceased sales of the products. Unfortunately, by that time, almost 100,000 of the systems had been implanted in patients worldwide. DePuy Orthopaedics, Inc. is the orthopedic subsidiary of Johnson & Johnson. DePuy has been called the most serious and widespread failure of a medical device to date.

The Facts

In March of this year, the New York Times published an article about the high early failure rate of DePuy’s ASR hip replacement. Since that article was published many more reports of failures of ASR hip replacements have been received by both DePuy and the United States Food and Drug Administration. In its article, the New York Times quoted orthopedic experts critical of the design of the ASR hip replacement. Experts were also critical of DePuy’s failure to stop sales of the device sooner.

 What Should you Do if you have a failed DePuy Hip Replacement ?

If you have a DePuy ASR hip replacement or hip resurfacing, and are experiencing problems with the device, call the DePuy Hip Replacement Helpline and speak to a DePuy Recall attorney immediately. You should retain an attorney before undergoing a revision surgery so that potentially important evidence can be preserved.  There is a limited period of time in which you may bring a legal action against DePuy for a failed ASR hip system, so don’t delay. Contact the DePuy Hip Replacement Helpline  today.

In March of this year, the New York Times published an article about the high early failure rate of DePuy’s ASR hip replacement. Since that article was published many more reports of failures of ASR hip replacements have been received by both DePuy and the United States Food and Drug Administration. In its article, the New York Times quoted orthopedic experts critical of the design of the ASR hip replacement. Experts were also critical of DePuy’s failure to stop sales of the device sooner.

If you have a DePuy ASR hip replacement or hip resurfacing, and are experiencing problems with the device, call the DePuy Hip Replacement Helpline and speak to a DePuy Recall attorney immediately. You should retain an attorney before undergoing a revision surgery so that potentially important evidence can be preserved.  There is a limited period of time in which you may bring a legal action against DePuy for a failed ASR hip system, so don’t delay. Contact the DePuy Hip Replacement Helpline  today.

Lawsuits are Being Filed against the Manufacturers of the DePuy

DePuy Hip Replacement lawyers are filing lawsuits against hip replacement manufacturers DePuy Orthopaedics, Inc over failure of a DePuy ASR metal-on-metal hip replacement. The lawsuit against DePuy was filed in Federal District Court in Ft. Myers, Florida . This is believed to be the first lawsuit filed in the United States over the failure of the DePuy ASR hip replacement.

Call the DePuy Hip Replacement Helpline and speak to a Medical Social Worker about you faulty DePuy. DePuy Hip Replacement lawyers are accepting cases fro victims of failed DePuy Hip Replacements and Metal toxicity complications.

The DePuy lawsuit alleges that the DePuy ASR hip replacement was defectively designed. It claims DePuy knew that their ASR hip replacements were failing at a higher than expected rate, yet it did not pass that information on to consumers or orthopaedic surgeons. As a result, diagnosis that the ASR hip replacement implanted in the patient has failed was needlessly delayed as her physicians were unaware of the prevelance of other failures. During the patient’s surgery to replace the failed hip replacement, her orthopedic surgeon discovered that the cup portion of the ASR hip replacement was extremely loose. The ASR hip replacement is designed so that a patient’s bone grows into the back of the cup to secure it. However, loosening because of a lack of bone in-growth into the cup is a hallmark of DePuy ASR hip replacement failures.

Unfortunately, DePuy’s recall of the ASR systems comes too late for patients that were implanted with these devices. This is not a typical recall where the toy with lead paint can simply be discarded or returned to the manufacturer for a refund. This recall is for a product that has been implanted in a person’s hip. As a result, the recalled product can only be replaced with the patient going through a painful and debilitating surgery and rehabilitation. In addition there are concerns about toxicity from the metal components rubbing. Patients are advised to have their blood levels checked for Chromium and Cobalt levels.

Many observers expect this already high failure rate to increase dramatically as problems with the DePuy ASR hip systems become more widely publicized. Denying that its decision to do so was related to reports of failures of the ASR systems, late last year DePuy ceased sales of the products. Unfortunately, by that time, almost 100,000 of the systems had been implanted in patients worldwide. DePuy Orthopaedics, Inc. is the orthopedic subsidiary of Johnson & Johnson.

Complications and Symptoms

In March of this year, the New York Times published an article about the high early failure rate of DePuy’s ASR hip replacement. Since that article was published many more reports of failures of ASR hip replacements have been received by both DePuy and the United States Food and Drug Administration. In its article, the New York Times quoted orthopedic experts critical of the design of the ASR hip replacement. Experts were also critical of DePuy’s failure to stop sales of the device sooner.

If you have a DePuy ASR hip replacement or hip resurfacing, and are experiencing problems with the device, call the DePuy Hip Replacement Helpline and speak to a DePuy Recall attorney immediately. You should retain an attorney before undergoing a revision surgery so that potentially important evidence can be preserved.  There is a limited period of time in which you may bring a legal action against DePuy for a failed ASR hip system, so don’t delay. Contact the DePuy Hip Replacement Helpline  today.

Call the Depuy Hip Replacement Helpline Oregon and speak to a Medical Social Worker and be connected to a Depuy Hip Replacement lawyer.

 

History

On August 2010 Johnson and Johnson did a voluntary recall of the DePuy ASR XL Acetabular System total hip replacement and the ASR Hip Resurfacing System.  It  has become evident over time  that DePuy Orthopaedics, a division of Johnson & Johnson, may have known about the complications  with theses devices as early as 2007. Tests  resulting in complications from an Australian study resulted in the company  pulling the devices off the market in Australia.

In March 2010, a letter was sent to doctors informing them about the serious complications regarding the Depuy hip prothesis.  Patients were not directly informed until the recall occurred in August 2010.

Thousands of patients are now seeking compensation from DePuy for medical bills and additional expenses associated with the faulty hip Implants. Tghis has effected a vulnerable senior population. Speak to a Depuy Hip Replacement lawyer today.
Find a Depuy Hip Replacement Lawyer for your faulty hip replacement today.

Depuy Hip Replacement lawyers and the DePuy Hip Replacement Helpline  are helping people with painful side effects associated with the DePuy ASR XL Acetabular System total hip replacement and the ASR Hip Resurfacing System:

Complications of the Depuy Hip Replacements

Metallosis: Characterized by rashes and nerve damage, metallosis is a condition that can occur when the metal-on-metal movement of the implant causes friction and releases higher, potentially dangerous levels of chromium and cobalt ions into the body.
Loosening of Hip Implant: The complication may cause patients to experience limping and difficulty walking. This often prompts the patient to transfer too much weight to the other hip or joints, resulting in additional pain and possible joint or bone failure.
More Surgery: Many of the side effects associated with the DePuy ASR devices require a patient to undergo additional hip replacement surgeries. Unfortunately, each additional surgery typically has a shorter life span than the previous replacement surgery.

Summary of Complications

  • Pain in the groin, hip or leg
  • Swelling at or near the hip joint
  • A limp or change in walking ability
  • Continued pain
  • The need for a second surgery
  • The need for tests and medical monitoring of Cobalt and Chromium levels in the bloodstream
  • Costly medical bills
  • Loss of enjoyment of certain activities
  • Pain
  • Leg length differences after revision surgeries
  • Lack of enjoyment of activities
  • loss of quality of life
  • Popping
  • Grinding
  • Metal sensitivity
  • Loosening of the prosthesis
  • Infection
  • Dislocation
  • Bone fracture
  • High metal ions levels in their bloodstreams

Cobalt Toxicity Hip Implant Alert

If you have a DePuy Hip replacement you must check your blood levels for high levels of Chromium and Cobalt. A high level of toxicity is characterized by symptoms of vision impairment, hearing loss, pain, swelling, and “brain fog.” This toxicity can cause allergic reactions and even death.

 

COBALT POISONING SYMPTOMS

  •     Gastrointestinal Problems
  •     Neuropathy (nerve damage)
  •     Thyroid Problems
  •     Kidney Failure
  •     Skin Disorders
  •     Hemorrhage
  •     Pulmonary Syndrome

  CHROMIUM POISONING CAN CAUSE

  •     Elevated Cancer Risks
  •     Reproductive System Problems
  •     DNA Mutations
  •     Impaired Liver Function

If You are contacted by Johnson and Johnson

You may have received correspondence from Depuy regarding  the recalled  DePuy ASR XL Acetabular System or ASR Hip Resurfacing System.  Prior to seeing a doctor, having additional surgery  or signing any paperwork provided by DePuy and/or Johnson & Johnson you must consult with a Depuy Hip Replacement lawyer. Be careful about signing any waivers from the Hip replacement manufacturers. Call the DePuy Hip Replacement Helpline and speak to our medical social worker and a DePuy Hip Replacement lawyer today.

Currently DePuy is providing some compensation to patients following the recall of the ASR devices, but the compensation is not comprehensive and may not cover expenses incurred following hip replacement surgery. The compensation and does not cover many diagnostic tests or blood tests that may be required to ensure a patient is healthy and to check for metallosis. Contact the  DePuy Hip Replacement Helpline to speak to a medical social worker and for a Depuy Hip Replacement lawyer and protect your right. Be compensated for your pain and suffering, additional surgeries, medical expenses and loss of quality of life.  The basic enjoyments of life can be put to a stop by a defective hip implant. Additional surgeries means more Rehabilitation, pain, suffering and lack of mobility. Chromium and Cobalt metal toxicity is an additional concern needing continuous blood analysis for toxic levels. The DePuy Implant has effected over 93,000 people.

What you need to do

  • If you are having complications see your Orthopedic surgeon immediately. Your health is first priority,
  • If you are not having complications and you have a Metal on Metal DePuy Hip Replacement get tested for chromium and cobalt levels in the bloodstream on a regular basis
  • Call the DePuy Hip Replacement Helpline for a lawyer. Speak to our medical social worker who speaks to people just like you with failed DePuy Hip Replacements. You are not alone. Thousands of DePuy ASR victims are facing the possibility of hip replacement complications and a painful and risky additonial surgeries to replace it. You must protect your rights, potential costly medical bills, pain and suffering and loss of  quality of life. You must send a message to the manufacturer.

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DePuy Hip Replacement Helpline lawyers

Are filing lawsuits on Behalf of Victims with the failed Depuy Hip Replacement devices. If you or a loved one is suffering do to a failed DePuy and needs additional revision surgeries contact the DePuy Hip Replacement Helpline lawyers for a case review for:

  •  Compensatory damages
  •  Medical Bills
  •  Pain and suffering
  •  Rehabilitation expenses
  •  Metal Toxicity compensation
  •  Loss of consortium
  •  Loss of quality of life
  •  Punitive damages

New Hip replacement Recall

 STRYKER HIP REPLACEMENT RECALL
Stryker Orthopaedics Recalls Rejuvenate Modular Hip System

In July 2012, Stryker Orthopaedics voluntarily recalled its Rejuvenate Modular Hip System. The recall includes both Stryker’s Rejuvenate Modular and ABG II modular-neck hip stems.
Risks

possible fretting and/or corrosion at the modular-neck junction, which may result in pain and/or swelling.

risks

  •     Joint loosening/dislocation
  •     Device wear and tear, such as corrosion and fretting
  •     Excessive metal debris leading to metal ion generation
  •     Inflammation of tissue
  •     Hypersensitivity/allergic response
  •     Broken devices