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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.
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Case Description*
Please explain exactly what happened, trying to state
as thoroughly as possible who you believe was responsible
and why you believe that person was negligent:
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Click on Your Model to Contact an Attorney
Guidant Recall Defibrillators |
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Guidant Pacemakers Recalled |
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Guidant CRT and Defibrillator Model Numbers: |
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Guidant Pacemaker Model Numbers Recalled: |
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0470
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0476
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0481
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0870
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0970
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0972
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0976
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0981
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1170
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1171 |
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1172
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1174
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1175
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1176
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1180
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1181
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1184
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1186
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1187
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1241 |
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1270
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1272
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1273
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1274
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1275
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1276
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1280
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1283
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1284
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1285 |
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1286
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1349
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1380
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1384
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1385
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1480
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1483
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1484
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1485
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1499 |
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CRT |
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Contak Renewal
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Contak Renewal 2
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Contak Renewal 3 (Class II)
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Contak Renewal 4 (Class II)
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Contak Renewal Model H135 (Class I)
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Contak Renewal Model H155 (Class I) |
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Renewal AVT (Class II)
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Renewal 3 AVT (Class II)
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Renewal 4 AVT (Class II)
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Renewal RF (Class II) |
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Sheff Law Offices, P.C. 10 Tremont Street Boston, MA 02108 (888) 423-4477
Also Investigating: Fosamax Osteonecrosis, Ketek Liver Injuries & Whistle-blower Qui Tam claims
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