What We Do
Defective Medical Products
- Medtronic Defibrillator Leads
- Medtronic Lawsuit
- Medtronic Lawyer
- AMO Complete Moistureplus Recall
- Botox
- Chromium Poisoning (Toxicity)
- Compounding Pharmacy Error
- Fentanyl
- Fentanyl Lawsuit
- Fentanyl Patch Recall
- Fleet Lawsuit - Phosphate Nephropathy Kidney Failure
- Fleet Renal Failure
- Fleet Phospho-Soda Kidney Failure
- Fleet Phospho-Soda Recall
- Fleet Recall
- Fleet Kidney Failure
- Fleet Laxative Lawsuit
- Fleet Phospho-Soda Lawsuit
- Fosamax Osteonecrosis Jaw
- Hydroxycut Lawsuit
- Hydroxycut Recall
- Levaquin Lawsuit
- NuvaRing Death
- Organon NuvaRing Lawsuit
- Ortho Evra Birth Control Patch
- Selenium Poisoning (Toxicity)
- Total Body Formula Recall and Lawsuit
- Trasylol and Kidney Failure
- Trasylol - Lawyer and Lawsuit
- Trasylol Recall
- Medtronic Defibrillator Leads
- Medtronic Lawsuit
- Medtronic Lawyer
- FDA Recalls
- News & Topics
Welcome to PritzkerOlsen, P.A.
MEDTRONIC LAWYER AND ATTORNEY
Pritzker | Olsen, P.A. is representing clients injured by defective Medtronic defibrillator leads. Several of our clients were shocked numerous times before their defibrillators were turned off. The firm has a national reputation in the area of product liability, and lawyers at the firm have been interviewed by The New York Times, The Wall Street Journal, Lawyers USA and other publications. To contact the firm, please call 1-888-377-8900 (toll-free), e-mail our managing Medtronic Lead lawsuit attorney, or submit our free case consultation form.
Medtronic Inc. has removed its Sprint Fidelis defibrillator leads from the market because they may fracture. Defibrillators are used to treat abnormal heart rhythms that can cause the heart to stop suddenly. They shock the heart back into normal rhythm by sending a pulse of energy through an electronic wire or lead that is connected to the heart. A defibrillator lead connects the defibrillator, which is implanted near the shoulder, to the heart. If a lead fractures, it may send false signals to the defibrillator, causing the defibrillator to deliver unnecessary shocks or, in some cases, not to pace or shock when needed. Read about the Medtronic Defibrillator Lead recall.
We represent people who were shocked multiple times when their Medtronic defibrillator leads fractured. The uncontrollable shocks continued until they arrived at emergency rooms where medical professionals could turn the defibrillators off. Two of our clients were shocked over twenty times.
"Cardiologists prefer defibrillator leads that are more flexible, which means thin and more likely to fracture. In an effort to capture more of the market share, Medtronic went too far. Medtronic Sprint Fidelis leads are so thin that they are fracturing at twice the rate of other defibrillator leads. Now Medtronic consumers are paying the price," stated Medtronic attorney Elliot Olsen.
If you are interested in being represented in a Medtronic lawsuit, please contact Elliot Olsen, our managing attorney for the Medtronic recall cases, or another Medtronic lawyer at the firm. To contact Elliot, please call toll-free at 1-888-377-8900 or submit the firm’s online consultation form.
Medtronic Sprint Fidelis Update:
Medtronic Sprint Fidelis Death
In a letter to doctors dated March 13, 2009, Medtronic Inc. told doctors that 13 deaths may be associated with the Medtronic Sprint Fidelis lead and that 4 of these deaths were associated with lead extraction.
We are representing the family of a man who died as a result of getting his Medtronic Sprint Fidelis lead removed. A young man, he left behind two young sons. We are fighting to obtain compensation for the family via product liability and medical malpractice claims. Read about heart lead extraction surgery malpractice.
DO YOU HAVE A MEDICAL MALPRACTICE CLAIM FOR NEGLIGENT REMOVAL OF A MEDTRONIC DEFIBRILLATOR LEAD?
Contact a lawyer about a medical malpractice lawsuit after injury or death from Medtronic lead removal (extraction) surgery >>
Keywords: Medtronic, lawyer, Sprint Fidelis lead, attorney, Medtronic lead extraction death, Medtronic Sprint Fidelis lead shock, patient shocked when Medtronic Sprint Fidelis fractured.
Note: Elliot Olsen is an attorney with Pritzker | Olsen, P.A.. He is a "Medtronic attorney" in the sense that he is handling Medtronic defibrillator lead claims. He does not work for Medtronic.
Free Case Consultation
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.
Attorney Elliot Olsen Speaks at Conference
Attorney Elliot Olsen recently spoke at the Seventh Annual LifeScience Alley Conference in Minneapolis on Preemption and the Future of Medical Device Litigation. He appeared with Randall Pattee of Lindquist and Vennum and Jean Lance, VP of corporate legal and general counsel for Boston Scientific.
ADHD Medication and Cardiac Death
ADHD Medications that may be associated with sudden death in healthy children, according to the FDA: Focalin, Focalin...
Zicam Lawsuits
On June 16, 2009 FDA altered consumers to the risk of anosmia (loss of smell) with the use of certain Zicam products marketed by Matrixx Initiatives. ...
Denture Cream Lawsuit
Denture users throughout the nation are suing denture cream manufacturers Proctor & Gamble Co. and GlaxoSmithKline PLC, alleging that Fixodent ...
Super PoliGrip Lawsuit
People who use dentures should be aware that lawsuits have been filed alleging that use of PoliGrip and other denture creams caused zinc poisoning, wh...
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.
NuvaRing Death
Lawsuits have been filed alleging death and serious injury associated with NuvaRing, a contraceptive product make by Organon. Contact us about NuvaRing stroke, NuvaRing pulmonary embolism, NuvaRing heart attack, and an Organon NuvaRing lawsuit.
