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Defective Medical Device Recalls: Pacemakers and Defibrillators
Pacemaker & Defibrillator Recall Listings


Guidant Defibrillators & Pacemakers

The following devices manufactured from Oct 27, 1997 to Dec 5, 2000.

• Contak TR - Model 1241
• Discovery - Models 1174, 1175, 1273, 1274 and 1275
• Discovery II - Models 0481, 0981, 1184, 1186, 1187, 1283, 1284, 1285 and 1286
• Intelis II - Models 1349, 1384, 1385, 1483, 1484, 1485 and 1499
• Meridian - Models 0476, 0976, 1176 and 1276
• Pulsar - Models 0470, 0870, 0970, 0972, 1172 and 1272
• Pulsar Max - Models 1170, 1171 and 1270
• Pulsar Max II - Models 1180, 1181 and 1280
• Virtus Plus II - Models 1380 and 1480

The following devices manufactured on or before Apr 16, 2002.

• Contak Renewal - Model H135
• Contak Renewal 2 - Model H155
• Ventak Prizm 2 DR - Model 1861

The following devices regardless of when manufactured.

• Contak Renewal 3 - Models H155, H170, H173 and H175
• Contak Renewal 3 AVT - Models M150 and M155
• Contak Renewal 3 AVT HE - Models M157 and M159
• Contak Renewal 3 HE - Models H177 and H179
• Contak Renewal 4 - Models H190 and H195
• Contak Renewal 4 AVT - Models M170 and M175
• Contak Renewal 4 AVT HE - Models M177 and M179
• Contak Renewal 4 HE - Models H197 and H199
• Insignia AVT DDD - Model 0982
• Insignia AVT DR - Model 1292
• Insignia AVT SR - Model 1192
• Insignia AVT SSI - Model 0482
• Insignia AVT VDD - Model 0882
• Insignia Entra DDD - Models 0985 and 0986
• Insignia Entra DR - Models 1294, 1295 and 1296
• Insignia Entra SR - Models 1195 and 1198
• Insignia Entra SSI - Models 0484 and 0485
• Insignia Plus DR - Models 1297 and 1298
• Insignia Plus SR - Model 1194
• Insignia Ultra DR - Models 1290 and 1291
• Insignia Ultra SR - Model 1190
• Nexus AVT DDD - Model 1432
• Nexus AVT DR - Model 1492
• Nexus AVT SR - Model 1392
• Nexus AVT SSI - Model 1328
• Nexus AVT VDD - Model 1428
• Nexus Entra DDD - Models 1425 and 1426
• Nexus Entra DR - Models 1466, 1494 and 1495
• Nexus Entra SR - Models 1395 and 1398
• Nexus Entra SSI - Models 1325 and 1326
• Nexus Plus DR - Models 1467 and 1468
• Nexus Plus SR - Model 1394
• Nexus Ultra DR - Models 1490 and 1491
• Nexus Ultra SR - Model 1390
• Renewal 3 AVT
• Renewal 3 AVT HE
• Renewal 4 AVT
• Renewal 4 AVT HE
• Renewal RF - Models H230 and H235
• Renewal RF HE - Model H239
• Ventak AVT - Models A135 and A155
• Ventak Prizm AVT - Model 1900
• Vitality AVT - Models A135 and A155
• Vitality DS - Model T125
• Vitality DS VR - Model T135
• Vitality 2 DR - Model T165
• Vitality 2 VR - Model T175


Medtronic Defibrillators

The following devices manufactured from Apr 2001 to Dec 2003.

• InSync Marquis - Model 7277
• InSync II Marquis - Model 7289
• InSync III Marquis - Model 7279
• InSync III Protect Model 7285
• Marquis DR - Model 7274
• Marquis VR - Model 7230
• Maximo DR - Model 7278
• Maximo VR - Model 7232

The following devices regardless of when manufactured, unless otherwise stated.

• GEM (serial PIP-H or PJJ-H) - Model 7227CX, manufactured before Oct 15, 1999
• GEM DR - Model 7271, manufactured Nov 1997 to Dec 1998
• GEM II DR - Model 7273, manufactured before 2000
• GEM II VR - Model 7229CX, manufactured before Oct 15, 1999
• Micro Jewel II - Model 7223CX, implanted in 1997
• Sigma S - Models SS103, SS106, SS203 and SS306
• Sigma D - Model SD203
• Sigma DR - Models SDR203, SDR303, SDR306 and SD203
• Sigma SR - Models SSR203, SR303 and SR306
• Sigma VDD - Model SVDD303


St. Jude Medical Defibrillators

The following devices regardless of when manufactured, unless otherwise stated.

• Atlas DR - Models V-240 and V-242
• Atlas Plus DR/VR/HF - Models V-193, V-193C, V-243, V-340, V-341 and V-343
• Atlas VR - Model V-199
• Epic DR/HF - Models V-233, V-337 and V-338
• Epic Plus DR/VR/HF - Models V-196, V-196T, V-236, V-239, V-239T and V-350
• Photon DR - Model V-230, manufactured 2002 or earlier
• Photon Micro VR/DR - Models V-194 and V-232, manufactured 2002 or earlier



 

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