Guidant Recall
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Defective Guidant Pacemaker, Defective Pacemakers

The Guidant pacemaker products including PULSAR, PULSAR MAX, DISCOVERY, MERIDIAN, PULSAR MAX II, DISCOVERY II, VIRTUS PLUS II, INTELIS II and CONTAK TR, manufactured between November 25, 1997 and October 26, 2000 are potentially defective.

MEDTRONIC NEWS

Medtronic Sprint Fidelis Leads Recalled

On Oct. 15, 2007, Medtronic suspended all sales of Sprint Fidelis leads. Please click here to read more about the Medtronic recall.

These products may not be properly sealed, resulting in a higher than normal moisture content within the pacemaker late in the pacemaker's usable service life.

The average implant life is 69 months, and the product failures have been noted after 44 months of implant life.

This failure mode could lead to one of the following:

  • Premature battery depletion
  • Inappropriate pacing function
  • Appearance of a reset warning
  • Inappropriate early display of replacement indicators

Of the 78,000 defective pacemaker products distributed, 28,000 remain implanted (18,000 in the United States). As of July 11, 2005, a total number of 69 devices have exhibited a failure.

The table below shows the model numbers with this potential defect. They are subject to the Guidant recall.

Defective Guidant
Pacemaker Products

Model Numbers

PULSAR MAX
 
PULSAR
 
DISCOVERY
 
MERIDIAN
 
PULSAR MAX II
 
DISCOVERY II
 
 
CONTAK TR
 
VIRTUS PLUS II
 
INTELIS II

1170, 1171, 1270
 
0470, 0870, 0970, 0972, 1172, 1272
 
1174, 1175, 1273, 1274, 1275
 
0476, 0976, 1176, 1276
 
1180, 1181, 1280
 
0481, 0981, 1184, 1186, 1187, 1283,
1284, 1285, 1286
 
1241
 
1380,1480
 
1483, 1484, 1485, 1384, 1385, 1349,
1499

Guidant recommends that physicians follow up with patients who have received one of these potentially defective pacemakers.

Back to list of Guidant defective products. Or read a summary of the Guidant recall.

About the Sponsors of this Pacemaker and Defibrillator Information Website

If you or a loved one has been injured due to a defective pacemaker or defibrillator product manufactured by Guidant, you may be entitled to compensation. The sponsors of this website are attorneys who specialize in helping those who have been injured by defective products. Please contact our offices today so that one of our Guidant lawyers may answer any questions that you have and provide a free case review if needed. Our toll-free number is 888-255-AWKO (2956). If warranted, we can file a Guidant lawsuit to help obtain the proper compensation.

The sponsors of this website include: Aylstock, Witkin & Sasser, Guidant Litigation Group; Neblett, Beard & Arsenault; Andrus, Boudreaux, Lemoine & Tonore; Lundy & Davis, LLP; and Barrios, Kingsdorf & Casteix, LLP.

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Guidant Pacemaker Recall     Guidant Defibrillators
Guidant FDA Safety Warnings     Guidant Defective Products
Guidant Defective Pacemakers     Guidant Lawsuits
Guidant Recall
 
VENTAK PRIZM 2 DR     CONTAK RENEWAL     VENTAK PRIZM AVT
VITALITY AVT     RENEWAL 3 AVT     RENEWAL 4 AVT
 
News: Boston Scientific purchases Guidant, issues recall of six more
Guidant pacemakers and defibrillators.

 
News: Medtronic recalls Sprint Fidelis leads used in patients with pacemakers.
 

Copyright 2005-2007 Aylstock, Witkin and Sasser. Site last updated November 30, 2007.
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