Guidant Recall
On June 17, 2005, Guidant issued a voluntary recall of its implanted cardiac defibrillator. The Guidant recall is linked to at least 45 failures of the device and the deaths of two patients.
Guidant Defibrulator Lawsuit

Guidant Recall Information
About Defibrillators
About Pacemakers
Contact an Attorney
FDA Recalls Guidant Pacemaker
Guidant Pacemaker Recall
Guidant Press Release
Health Related Links
Recalled Defribrillators
Recent FDA Updates Concerning Guidant

Claim Information
Heart Conditions and Diseases
Heart Health

 

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Conditions and Diseases

What is cardiovascular disease?

       Cardiovascular disease (CVD) is not one single disease or condition. It is a group of different disorders that affect your heart and blood vessels. You are born with some types of cardiovascular diseases, and you develop others during your lifetime.

       Learn more about specific cardiovascular conditions and diseases using the links below.

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Guidant Recall Defibrillators

 

Guidant Pacemakers Recalled

 

Guidant CRT and Defibrillator Model Numbers:

 

Guidant Pacemaker Model Numbers Recalled:

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

CRT

  • Contak Renewal
  • Contak Renewal 2
  • Contak Renewal 3 (Class II)
  • Contak Renewal 4 (Class II)
  • Contak Renewal Model H135 (Class I)
  • Contak Renewal Model H155 (Class I)
  • Renewal AVT (Class II)
  • Renewal 3 AVT (Class II)
  • Renewal 4 AVT (Class II)
  • Renewal RF (Class II)

 

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(888)423-4477
(617) 227-7000

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Sheff Law Offices, P.C.
10 Tremont Street
Boston, MA 02108
(888) 423-4477

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