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Guidant Defibrillator Recall
The manufacturer has announced that they will pay to replace 28,900 internal cardiac defibrillators, which cannot be fixed without removing the mini-cassette sized medical device. If you have one of the following devices installed, contact the product liability lawyers of Miller & Associates to ensure you receive the best medical treatment.
The following models of Guidant heart defibrillators have been recalled.
- Ventak Prizm 2 DR (Model 1861)
- Contak Renewal (Model H135)
- Contak Renewal (Model H155)
- Ventak Prizm AVT
- Vitality AVT
- Contak Renewal 3 AVT
- Contak Renewal 3 AVT HE
- Contak Renewal 4 AVT
- Contak Renewal 4 AVT HE
- Contak Renewal 3
- Contak Renewal 3 HE
- Renewal 3 AVT
- Renewal 3 AVT HE
- Contak Renewal 4
- Contak Renewal 4 HE
- Renewal 4 AVT
- Renewal 4 AVT HE
- Renewal RF
- Renewal RF HE
The law firm of Miller & Associates has a proven track record of achieving results for their clients in product liability cases. Learn more about their accomplishments here.
Product Liability Breaking News
"Guidant Heart Defibrillator Claims"
Boston Scientific Corp. has amended a settlement agreement involving faulty Guidant defibrillator claims to include an additional $45 million, bringing the total settlement amount to $2...
"FDA Urges Patients to Schedule Exam"
A statement released yesterday by the U.S. Food and Drug Administration urged patients with potentially defective models of Boston Scientific/Guidant pacemakers and defibrillators to schedule an exam with their physicians as soon as possible.
...
"Defibrillators May fail 10 times more than projected"
A U.S. Food and Drug Administration analysis found that Guidant defibrillators may fail as much as 10 times more than the company projected last year.
Guidant defibrillators have been implanted into thousands of cardiac patients and are used t...
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