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U.S. Department of Health and Human Services

Medical Device Recalls
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261 to 270 of 284 Results
Product: pacemaker
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Product Description
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FDA Recall
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Insignia Entra Multiprogrammable Pacemaker, DDDR Model 1298 2 05/29/2003 Guidant Corp-Cpi Division
Contak TR Multiprogrammable Pacemaker, DDDR Model 1241 2 05/29/2003 Guidant Corp-Cpi Division
Pulsar Multiprogrammable Pacemaker, DDD Model 970 2 05/29/2003 Guidant Corp-Cpi Division
Pulsar Multiprogrammable Pacemaker, DDD Model 972 2 05/29/2003 Guidant Corp-Cpi Division
Pulsar Multiprogrammable Pacemaker, DDD Model 976 2 05/29/2003 Guidant Corp-Cpi Division
Pulsar Multiprogrammable Pacemaker, DDDR Model 1270 2 05/29/2003 Guidant Corp-Cpi Division
Pulsar Multiprogrammable Pacemaker, DDDR Model 1272 2 05/29/2003 Guidant Corp-Cpi Division
Pulsar Max Multiprogrammable Pacemaker 2 05/29/2003 Guidant Corp-Cpi Division
Insignia Plus Multiprogrammable Pacemaker, DDD Model 985 2 05/29/2003 Guidant Corp-Cpi Division
Meridian Multiprogrammable Pacemaker, DDDR Model 1276 2 05/29/2003 Guidant Corp-Cpi Division
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