Medtronic Defibrillator Lead Recall Attorneys
Defibrillator Recalls
Medtronic Recall 101 Quick Facts
Category: Defibrillator Recalls
Sprint Fidelis Medtronic leads were recalled on October 15, 2007 after reports of at least five patient deaths associated with defibrillator leads.
The leads were found to be prone to cracking which can lead to potentially life threatening consequences.
Sprint Fidelis Defibrillator Lead Update
Category: Defibrillator Recalls
Six months have passed since Medtronic recalled its Sprint Fidelis defibrillator Model 6949 leads in October 2007.
Lawsuit Filed Against Medtronic for Sprint Fidelis Defibrillator
Category: Defibrillator Recalls
An Evansville woman claims a defibrillator wire implanted in her chest was supposed to detect and correct abnormal heart arrhythmias. But, in a federal lawsuit, the woman claims the device delivered painful shocks to her heart that led to her hospitalization.
The products liability lawsuit filed in the U.S. Southern District Court, claims Medtronic, the manufacturer, was aware of the problems in patients who had a Sprint Fidelis defibrillator lead wire (model no. 6949), implanted but did not remove the wires from the market until October.
Continue reading "Lawsuit Filed Against Medtronic for Sprint Fidelis Defibrillator"
Medtronic Recall Numbers - Sprint Fidelis Defibrillator Leads
Category: Defibrillator Recalls
When people see the news about Medtronic's defective defibrillators, it sparks concern and alarm. In an automotive defective products recall, we know the make and model of our cars.
However, most people usually don't know the serial numbers or model numbers of their defibrillators, and will have to research their medical records or speak with the helathcare provider to determine if they have a defective medical device, or potentially defective device. They want to know - is MY defibrillator defective? Is it included in the recall? Sometimes, the fear is unwarranted.
The Medtronic Defibrilator Recall includes: Sprint Fidelis Defibrillator Leads with the following model numbers: 6930, 6931, 6948 and 6949, all manufactured by Medtronic, from the month of September, 2004 through the month of October 15, 2007.
If you have one of these and would like to know what to do, please fill out the form at right.
Medtronic Recalls Defibrillator Leads
Category: Defibrillator Recalls
Sprint Fidelis, a popular heart defibrillator model has been recalled due to a defect that may have contributed to five deaths.
The defect is an electrical wire in the Sprint Fidelis, manufactured by Medtronic, which can cause the device to deliver unnecessary electric shocks to the heart or fail to shock when needed. Medtronic estimates 4,000 to 5,000 people will experience a problem with the wire during the first 30 months of use.
Medtronic Sends Letter to Patients
Category: Defibrillator Recalls
Medtronic recently sent a letter to doctors with important information regarding their Sprint Fidelis defibrillation leads.