NOTE: Labels in bold are required.
Medtronic Sprint Fidelis Defibrillation Leads
Model numbers 6930, 6931, 6948 and 6949
Contact a Sprint Fidelis defibrillation leads attorney now
Charleston, West Virginia
From: MEDWATCH - The FDA Safety Information and Adverse Event Reporting
Medtronic voluntarily suspends distribution of its Sprint Fidelis defibrillation leads because a small number of fractures have been detected
FDA issued a statement announcing Medtronic's decision to voluntarily suspend distribution of its Sprint Fidelis defibrillation leads because a small number of fractures have been detected. As a result of Medtronic's action, no more Sprint Fidelis leads will be sold or manufactured and any remaining product should be pulled from inventory and returned to the company.
When a defibrillator lead is slightly more prone to fracture, most leads will function well, as is the case with Sprint Fidelis. In the infrequent circumstance where a lead actually breaks, or "fractures," the lead may send false signals that cause inappropriate defibrillator shocks, or therapies such as pacing or shocks may not be delivered.
Current adverse event information indicates that fractures have occurred in less than 1 percent of the approximately 268,000 of these leads implanted worldwide. Patients who are implanted with this lead are encouraged to contact their physicians for further information.
Read the complete MedWatch 2007 Safety Summary including a link to the FDA Statement and Consumer Questions and Answers, at:
http://www.fda.gov/medwatch/safety/2007/safety07.htm#Fidelis
Additional Resources:
Important Patient Information Sprint Fidelis Lead Performance from Medtronic
Class 1 Recall: Medtronic Inc. Sprint Fidelis® Defibrillator Leads - USDA
Free Consultations Available
Don't be intimidated by big pharmaceuticals or medical device companies. Put the law in your hands - contact defective drug attorneys and medical device recall lawyers at The Bell Law Firm, PLLC today. Located in Charleston, we represent clients throughout West Virginia, including Huntington, Parkersburg, Bluefield, Williamson, Morgantown, Fairmont, Martinsburg, Beckley and the entire state of West Virginia.
Establishing the Facts
As your legal representation, The Bell Law Firm, PLLC develops and presents evidence linking your injuries to the use of a particular medical product. Given the fact that recalls have already occurred in the case of many of these products, facts already exist in evidence regarding their dangers. In order to counter defense arguments claiming injuries were caused by a pre-existing condition or factors unrelated to their product, our personal injury attorneys consult with medical doctors and medical device experts, submitting evidence and proof in support of your case.
Bell Law Firm is presently taking Sprint Fidelis defibrillation leads cases, and we will work hard to obtain compensation for your side effects and suffering. Please fill out our contact form and a representative from Bell Law Firm will be in contact with you as soon as possible.
