Delaware Medtronic Class Action Heart Lead Recall Lawsuit Attorney Lawyer ICD Delaware | Latest News DE
If you live in Delaware and need to talk to a Medtronic Sprint Fidelis lead recall attorney, please contact our Delaware Medtronic Class Action Lawsuit Team for a free consultation. If you or a loved one has suffered from a defective lead, fractures, unnecessary shocks or has died from defective Medtronic leads you may be entitled to compensation.
If you have any questions regarding the Sprint Fidelis defibrillation leads models 6930, 6931, 6948, 6949 we can help provide you with the latest legal updates and news. Please call or contact us via e-mail for a confidential free consultation regarding your legal options.
Below is a directory of hospitals in Delaware. If you have questions regarding Sprint Fidelis Medtronic heart leads and your medical options it is important to contact a doctor that can help answer your questions.
Delaware Hospitals
Alfred I duPont Hospital
1600 Rockland Road
Wilmington, DE 19803-3616
(302) 651-4000
Bayhealth Medical Center
640 South State Street
Dover, DE 19901-3597
(302) 674-4700
Beebe Medical Center
424 Savannah Road
Lewes, DE 19958-0226
Christiana Care Health System
4755 Ogletown-Stanton Road
Newark, DE 19718-0002
(302) 733-1000
Delaware Psychiatric Center
1901 North Dupont Highway
New Castle, DE 19720-1199
(302) 255-2700
Meadow Wood Behavioral Hlth
575 South Dupont Highway
New Castle, DE 19720-4600
(302) 328-3330
Nanticoke Memorial Hospital
801 Middleford Road
Seaford, DE 19973-3698
(302) 629-6611
Rockford Center
100 Rockford Drive
Newark, DE 19713-2121
(302) 996-5480
Select Specialty Hospital
7 Clayton Street, 5th Floor
Wilmington, DE 19801
(302) 421-4545
St Francis Hospital
Seventh and Clayton Streets
Wilmington, DE 19805-0500
(302) 421-4100
Veterans Affairs Med Center
1601 Kirkwood Highway
Wilmington, DE 19805-4989
(302) 994-2511
Delaware hospital directory published by the Fields Law Firm Medtronic Sprint Fidelis lead recall attorneys.
We are a law firm dedicated to helping those injured by Medtronic Sprint Fidelis Defibrillator Lead.
Medtronic Recall Lawsuit
- Medtronic 6931 Lead Fractures | Fidelis 6931 Leads Recall Lawsuit
- Sprint Fidelis 6949 Defibrillator Leads | Medtronic Recall Lawsuit
- Medtronic Recall Class Action Lawsuit Information
- Medtronic Sprint Fidelis 6949 Lawsuit Class Action Recall Updates | Attorney Lawyer
- Sprint Fidelis Lawsuit Status | FDA News Lead Fractures
- Medtronic FDA Recall | Sprint Fidelis Lawsuit News
- Sprint Fidelis Lawsuit Status | Medtronic Recalls Heart Leads
U.S. Food & Drug Administration Statement On Medtronic Sprint Fidelis Defibrillator
Medtronic Suspends Sprint Fidelis Defibrillation Leads (PDF)
U.S. FDA Class 1 Recall Report
If you or a loved one have been injured by the Medtronic Sprint Fidelis lead please contact us immediately. You may be entitled to compensation.
If you or someone you know has received a Medtronic 6931 defibrillator lead you may have important legal rights. Many heart patients have experienced a lead fracture which can cause painful and sometimes life-threatening shocks to the heart or alternatively not provide a shock when needed. We are currently representing patients who have defective Medtronic [...]
If you or someone you know has received a Sprint Fidelis defibrillator lead 6949 you may have important legal rights. Many patients have experienced a lead fracture which can cause painful and sometimes life-threatening shocks to the heart or alternatively not provide a shock when needed. We are currently representing patients who have a defective [...]
On October 15, 2007 a Medtronic recall was issued due to reports of at least five patient deaths linked with defective defibrillator leads. The heart leads are susceptible to fracture which can then cause the defibrillator to deliver unnecessary shocks or not operate at all. Following the recall no more Sprint Fidelis leads were sold [...]
The Minneapolis Heart Institute conducted a study of the Medtronic Sprint Fidelis 6949 lead and determined that the lead had a greater failure rate compared to the Quattro lead. In October 2007 Medtronic announced a recall of Sprint Fidelis lead 6949 along with leads 6948, 6930 and 6931.
Medtronic Lead Failure
Minneapolis Heart Institute Foundation Study
Early failure [...]
On September 4, 2008 the FDA released a News Alert regarding a software update from Medtronic that is supposed to help detect Sprint Fidelis lead fractures. Approximately 268,000 Sprint Fidelis lead have been implanted in patients worldwide. The Medtronic recall of heart leads included four Sprint Fidelis models: 6930, 6931, 6948 and 6949.
Recalls Sprint Fidelis
FDA [...]
