Lieff Cabraser Heimann & Bernstein, LLP is a national law firm that represents plaintiffs in individual actions and class action lawsuits. Please note: our firm is no longer accepting new clients in this litigation.
Medtronic Heart Lead Recall
News Article Excerpt
October 30, 2007
News Inferno.com, "Defective
Medtronic Sprint Fidelis Lead Fracture Reports Ignored by Company,
FDA for Months Prior to Recall"
Medtronic Inc. knew that its Sprint Fidelis
Defibrillator Leads were fracturing at higher-than-usual rates for months.
Yet, the company appears to have dragged its feet in getting the defective
Sprint Fidelis Lead off the market. Medtronic even went so far as to
blame physicians for the problems, claiming that they weren't implanting
the defective Sprint Fidelis Lead properly. What's even worse, the Food & Drug
Administration (FDA), which never required the defective medical device
to undergo clinical testing, was oblivious to the increasing reports
of Sprint Fidelis Lead problems.
Medtronic suspended sales of the Sprint Fidelis Leads in October, after
receiving reports of 5 fatalities linked to lead fractures. A lead is
a wire that connects an implantable defibrillator to the heart. When
it breaks, the defibrillator can emit a massive and painful shock. And
in the worse case scenario, the fractured lead can prevent a defibrillator
from sending a necessary, lifesaving shock to the heart. Replacing a
lead is not an easy procedure, as the invasive surgery can cause the
tissue of the blood vessels and heart to tear. In fact, replacing a defibrillator
lead is so risky that patients with Sprint Fidelis Leads are being told
to leave the defective components in place unless they fracture.
Founded in 1972, Lieff Cabraser Heimann & Bernstein,
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TRADEMARK NOTICE: "Sprint Fidelis" is
a trademark of Medtronic, Inc. Lieff Cabraser
is in no way affiliated with Medtronic, Inc. The use of this
mark is solely for informational and product identification purposes.