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Defective Medical Products
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Guidant CONTAK RENEWAL® Defibrillator Recall
On June 29, 2005, the Food and Drug Administration (FDA) announced a Class I recall of Guidant CONTAK RENEWAL®, Model H135, and CONTAK RENEWAL® 2, Model H155, Cardiac Resynchronization Therapy Defibrillators (CRT-Ds). (See the FDA Class I recall of Guidant CONTAK RENEWAL® defibrillators.) According to the FDA announcement, a deterioration in a wire insulator could cause a short circuit, resulting in the device’s inability to deliver an electric shock during episodes of arrhythmia (abnormal heart rhythm). This could cause serious injury or death. As of December 28, 2005, there have been 35 clinical failures of the CONTAK RENEWAL® Guidant Defibrillators. 5 of these people have died. (See information on the December 28, 2005, Guidant defibrillator update.)
If you or a loved one has one of these Guidant heart defibrillators you or the family member may:
- Want to have the CONTAK RENEWAL® Guidant defibrillator removed or
- Have experienced injury from a failure of the Guidant heart defibrillator.
Sadly, a family member may have died as a result of a Guidant defibrillator failure. In any of these cases, even if you only suspect an injury or death was caused by a Guidant defibrillator, lawyers at Pritzker | Ruohonen are available for a free consultation. You may be entitled to compensation from Guidant. Damages sought against Guidant could include compensation for physical and mental pain and suffering, medical and hospital expenses and punitive damages.
Guidant lawsuits involve complex medical, scientific, and legal issues. Attorney Fred Pritzker has 29 years of experience successfully fighting for the rights of injured people. During that time, he has focused his practice on complex cases, including defective medical device cases. As a testimony to his excellence, he has been selected for inclusion in the 2005-2006 edition of The Best Lawyers in America.
If you have questions about Guidant defibrillators, lawyers at Pritzker | Ruohonen can help. You can reach Attorney Fred Pritzker and the other lawyers at Pritzker | Ruohonen by calling toll-free at 1-888-377-8900, by emailing info@pritzkerlaw.com, or by filling out the online consultation form. Consultations are free.
Pritzker | Ruohonen has already filed suit against Guidant on behalf of people who had these Guidant implantable heart defibrillator devises implanted in their bodies. It will cost you nothing to talk to Fred Pritzker about your CONTAK RENEWAL® Guidant defibrillator, and it may result in the peace of mind you deserve. Pritzker | Ruohonen is a national law firm with offices centrally located in Minneapolis, Minnesota. We represent clients throughout the United States.
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Firm News
Fred Pritzker Listed in The Best Lawyers in America
Fred Pritzker has been notified that he will again be listed in The Best Lawyers in America for his work in personal injury litigation.
Pain and Suffering
Rich Ruohonen recently chaired a legal seminar on obtaining compensation for pain and suffering in a personal injury case. Rich uses his knowledge, experience, and reputation to maximize recoveries for clients.
Medtronic Recall and Medtronic Lawsuit
FDA has annonced a Medtronic Spring Fidelis defibrillator lead recall. Two of our clients with defective Medtronic leads were shocked over twenty times before medical professionals were able to turn off the defibrillator.
Fleet Lawsuit
We are representing several people who experienced kidney failure (acute phosphate nephropathy) after use of Fleet Phospho-soda solution or Fleet Accu-Prep solution for bowel cleansing.
Ortho Evra Lawsuit: Ortho Evra Birth Control Patch
The Ortho Evra birth control patch has been linked to an increased risk of blood clots that can lead to pulmonary embolism, stroke and heart attack.
Trasylol Recall
Bayer has agreed to a marketing suspension of Trasylol, a drug used to control bleeding during heart surgery, pending detailed review of preliminary results from a Canadian study that suggested an increased risk for death.
Fentanyl Lawsuit and Fentanyl Recall
There have been a number of recalls regarding fentanyl due to the risk of a fentanyl overdose.
Fosamax and Osteonecrosis
Several cases of bisphosphonate-associated osteonecrosis of the jaw have been associated with the use of oral bisphosphonates, including Fosamax®, Actonel®, and other medications.
