- Medical Malpractice
- Product
- Unsafe Drugs
- Bisphosphonate Litigation
- Bextra Litigation
- Silicone Gel Breast Implant Litigation
- Fen-Phen Diet Drugs
- Guidant Defibrillators
- Hormone Replacement Drugs
- Kugel Hernia Mesh Patches
- Medtronic Sprint Fidelis Lead
- Mentor ObTape Trans-Obturator Tape Litigation
- Ortho Evra Birth Control Patch
- Bausch & Lomb's ReNu with MoistureLoc Contact Lens Solution
- Vioxx Litigation
- Shoulder Pain Pumps
- Medtronic Defibrillator Litigation
- Other/Archive Drug Products
- Personal Injuries
- Auto Accidents
- Nursing Home Abuse
Medtronic Sprint Fidelis Lead
As of October 2007, physicians nationwide received an alert from Medtronic, Inc. with regard to certain of the manufacturer’s Sprint Fidelis leads. The recall was issued because of complications such as multiple shocks, lightheadedness, fainting, or palpitations due to fractures in the leads. Recalled Medtronic Sprint Fidelis Leads ID numbers begin with 6930, 6931, 6948 or 6949.
Alley, Clark, Greiwe & Fulmer is one of only a handful of firms that are becoming involved in litigation with Medtronic leads. Please contact our office immediately if you or someone you love has been received a Medtronic Lead.
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