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U.S. Department of Health and Human Services

Medical Device Recalls
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141 to 150 of 279 Results
Product: pacemaker
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Guidant INSIGNIA I Plus family of pacemakers includes the following: SR (model 1194); and DR (models... 2 11/23/2005 Guidant Corporation
Guidant INSIGNIA I Ultra family of pacemakers includes the following: SR (models1190); and DR (model... 2 11/23/2005 Guidant Corporation
Guidant INSIGNIA I Entra family of pacemakers includes the following: SSI (model numbers 0484 and 0... 2 09/24/2005 Guidant Corporation
Guidant INSIGNIA I Ultra family of pacemakers includes the following: SR (models1190); and DR (mo... 2 09/24/2005 Guidant Corporation
Guidant INSIGNIA I Plus family of pacemakers includes the following: SR (models1194); and DR (mod... 2 09/24/2005 Guidant Corporation
Guidant INSIGNIA I AVT family of pacemakers includes the following: SSI (model 482), VDD (model 88... 2 09/24/2005 Guidant Corporation
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
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