medtronic defibrillator recall

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medtronic defibrillator lead recall

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72 documents for medtronic defibrillator recall

- Medtronic Announces a Nationwide, Voluntarily Recall of Small Subset of Two Implantable Cardioverter-Defibrillator Models.
Business Editors/Health/Medical Writers MINNEAPOLIS--(BUSINESS WIRE)--April 16, 2004 Medtronic, Inc. today announced that it is voluntarily recall...
- Business Wire
- April 16, 2004
- 10 Detroit General Retirement v. Medtronic, Inc., (8th Cir. 2010)
... connects an internally implanted defibrillator to a patient's heart and delivers electricity if a... culminating with the company's decision to recall the device. Medtronic again stated the difference ...
- Federal Circuits
- Medtronic Recall Update: Answers to Frequently Asked Questions From Plaintiffs' Attorneys Representing Clients in Defective Medtronic Heart Lead Lawsuits.
..., for manufacturing defective defibrillator leads have issued a series of answers to frequentl...
- Business Wire
- October 25, 2007

- Life Sciences Newsbriefs: Week Of November 21, 2011 - Part 1.
.... Medtronic wins FDA approval for chronic pain device Medtroni...-Control, Medtronic's external defibrillator division, for $487 million in cash. The deal is ta.... FDA announces recall of surgical device over patient fall risk Reports ...
- Mondaq Business Briefing
- Nbr. 2011, January 2011
- The Medtronic Heat Lead Recall: Attorneys For Patients Provide Answers To Frequently Asked Questions.
..., for manufacturing defective defibrillator leads issued today a list of answers to common que...
- Business Wire
- October 22, 2007
- Medtronic Case Returns to West Virginia
Back in February 2006, the family of James A. LoFiego filed a medical malpractice lawsuit in federal court against Medtronic Inc., alleging the company's equipment made caused LoFiego's death. [...] it alleges that Medtronic violated the West Virginia Consumer Protection Act by engag(ing) in unfair competition or unfair, unconscionable, deceptive or fraudulent acts or practices LoFiego's lawsuit, which requests a jury trial, also accuses the company of unjust enrichment for accepting money and payment from LoFiego, other patients, doctors, hospitals and insurance companies for defective equipment.

... to receive an implantable cardiac defibrillator and a cardiac resynchronization therapy device. Im... announced April 4, 2004, that it was recalling two models of cardiac devices made by Medtronic, t...
- State Journal, The
- August 25, 2009
- Class Counsel Announce Patients File Class Action Lawsuit Against Medtronic For Manufacturing Faulty Defibrillator Lead Wires.
... Expenses Arising Out Of The Medtronic Recall . MINNEAPOLIS, Minn. & SAN JUAN, Puerto Rico -- Cl...
- Business Wire
- October 15, 2007
- Heart Implant Manufacturer Recalls 50,000 Cardiac Defibrillators
Calls from terrified patients came pouring in shortly after cardiovascular product manufacturer Guidant recalled nearly 50,000 cardiac defibrillators, said Dr. Freddy Abi Samra, medical director of the Ochsner Clinic Foundation's electrophysiology laboratory. The first few calls I got were from people who thought the devices were actively killing people all over the country, Abi Samra said.

... market, behind only Minneapolis-based Medtronic with 49 percent. Since the recall was announced, T...
- New Orleans City Business
- August 08, 2005
- Kentucky Resident Files Lawsuit Against Medtronic For Faulty Defibrillator Lead Wire That Caused Devastating Electrical Shocks.
... comply with this duty with regard to the recalled lead wires. The Medtronic Sprint Fidelis lead has ...
- Business Wire
- November 28, 2007
- Life Sciences Newsbriefs: Week Of March 7, 2011
... Cook Medical gets Class I recall notice for catheter components The FDA has ordered... Medtronic ends contract with Premier for spinal devices Medt... system maker Medtronic's heart defibrillator unit, Physio-Control, has bought Jolife, a Swedish...