What We Do
Defective Medical Products
Welcome to Pritzker | Ruohonen
Guidant Pacemaker Recall
At the law firm of Pritzker | Ruohonen & Associates, P.A., we represent people across the United States in actions against biomedical companies for injuries and death caused by defective medical devices. Recently, Guidant Corporation has recalled certain models of Guidant pacemakers. Our attorneys understand the pain and uncertainty this has caused Guidant heart device patients, and we are here to help patients understand their legal rights and Guidant’s legal responsibilities for selling potentially defective Guidant pacemakers. Attorney Fred Pritzker has had 29 years of experience getting results for clients and has been named, once again, a Top 100 Super Lawyer. He has also been selected for inclusion in the 2005-2006 edition of The Best Lawyers in America.
If you or someone you love has had a Guidant pacemaker removed or is considering that option, the attorneys at Pritzker | Ruohonen are available to discuss your concerns. You can reach our attorneys for a free consultation by calling toll-free at 1-888-377-8900 or filling out our online Guidant free consultation form.
Fatality and Injuries Prompt Recall of Guidant Pacemakers
As of early July 2005, Guidant had received reports of 69 Guidant pacemaker failures. One death may be linked to a Guidant pacemaker that sustained pacing at an abnormally rapid rate. The models recalled include the following:
PULSAR® MAX Models 1170, 1171, 1270
PULSAR Models 0470, 0870, 0970, 0972, 1172, 1272
DISCOVERY® Models 1174, 1175, 1273, 1274, 1275
MERIDIAN® Models 0476, 0976, 1176, 1276
PULSAR MAX II Models 1180, 1181, 1280
DISCOVERY II Models 0481, 0981, 1184, 1186, 1187, 1283, 1284, 1285, 1286
CONTAK TR® Model 1241
VIRTUS PLUS® II* Models 1380, 1480
INTELIS II Models 1483, 1484, 1485, 1384, 1385, 1349, 1499
Guidant Not Willing to Pay for All Medical Expenses Incurred Due to Replacement of Guidant Pacemaker
Although Guidant has agreed to, under certain circumstances, replace the recalled Guidant pacemakers, Guidant has claimed it will pay only a limited amount of medical costs associated with the replacement. This puts a financial burden on patients wanting to have potentially defective Guidant pacemakers replaced.
At Pritzker | Ruohonen we have already filed a class action suit against Guidant on behalf of patients with defective Guidant defibrillators. If you have one of the recalled Guidant pacemakers or have recently had one replaced, our experienced attorneys will help you understand what legal actions you can take against Guidant to ensure the payment of all medical costs associated with replacement and to be compensated for loss of income and pain and suffering.
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.
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.
