Sprint Fidelis Leads:
Sprint Fidelis News:
If you or someone you know has received a Medtronic defibrillator since 2004, you need to be aware of faulty electrical lead wires (electrodes). These wires connect the heart to the heart defibrillator device. The wires are prone to fracture and can cause malfunctions of the device. » More About Defective Defibrillators
Medtronic, the nation’s largest maker of implanted heart devices, has advised all of the patients that received the Sprint Fidelis model leads (used in Sprint Fidelis Models 6930, 6931, 6948, and 6949) since 2004 to immediately see or contact their doctors for corrective actions, monitoring, or advice. » See if you have a Sprint Fidelis Defibrillator Lead Wire case
Download free PDF guide for more information about Faulty Electrical Leads Implantable Cardioverter Defibrillator Wires.
Please fill out the form below to see if you have a Sprint Fidelis Defibrillator Lead Wire case.
If you or a family member has suffered serious medical consequences from a faulty Medtronic defibrillator, Sprint Fidelis model– then you have a viable reason to consult with and retain a Pennsylvania law firm well versed in product negligence, personal injury, and wrongful death. Please contact Monheit Law for your free, no-obligation consultation today.
PERSONAL INFORMATION
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MEDICAL INFORMATION
| Which manufacturer's device has been implanted? | |
| What was the date you received your implant? | |
| Which model lead wires were used? | |
| If 'Other' Please Specify: | |
| Did your lead wires break or fracture? | Yes No |
| What complications have you had from the defibrillator leads (wires, electrodes)? | |
| Were your lead wires replaced or capped? | Yes No |
| What recommendations have your doctors made about replacing these wires (leads)? | |
| If wires replaced or implant removed, what was the date of removal or replacement of your implant or wires? | |
| Please be specific and tell us about your experience with the Defibrillator and Leads: | |
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