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U.S. Department of Health and Human Services

Medical Device Recalls
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151 to 160 of 284 Results
Product: pacemaker
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DISCOVERY (model nos. 1174, 1175, 1273, 1274 and 1275) pacemaker. Sterilized with gaseous ethylene ... 1 07/28/2005 Guidant Corporation
MERIDIAN (model nos. 476, 976, 1176 and 1276) pacemaker. Sterilized with gaseous ethylene oxide. ... 1 07/28/2005 Guidant Corporation
PULSAR and PULSAR MAX (model nos. 470, 870, 970, 972, 1170, 1171, 1172, 1270 and 1272) pacemaker. S... 1 07/28/2005 Guidant Corporation
PULSAR MAX II (model nos. 1180, 1181 and 1280) pacemaker. Sterilized with gaseous ethylene oxide. ... 1 07/28/2005 Guidant Corporation
DISCOVERY II (model nos. 481, 981 1184, 1186, 1187, 1283, 1284, 1285 and 1286) pacemaker. Steriliz... 1 07/28/2005 Guidant Corporation
VIRTUS PLUS II (model nos. 1380 and 1480) pacemaker. Sterilized with gaseous ethylene oxide. Gui... 1 07/28/2005 Guidant Corporation
INTELIS II (model nos. 1349, 1384, 1385, 1483, 1484, 1485 and 1499) pacemaker. Sterilized with gas... 1 07/28/2005 Guidant Corporation
CONTAK TR (Model no. 1241) pacemaker. Sterilized with gaseous ethylene oxide. Guidant Corporatio... 1 07/28/2005 Guidant Corporation
Discovery II Multiprogrammable Pacemaker, Model 1286 2 07/15/2003 Guidant Corp-Cpi Division
Pulsar Max II Multiprogrammable Pacemaker, Model 1280 2 07/15/2003 Guidant Corp-Cpi Division
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