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U.S. Department of Health and Human Services

Medical Device Recalls
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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Insignia Entra Multiprogrammable Pacemaker, DDDR Model 1297 2 05/29/2003 FEI # 2124215
Guidant Corp-Cpi Division
Insignia Entra Multiprogrammable Pacemaker, DDDR Model 1298 2 05/29/2003 FEI # 2124215
Guidant Corp-Cpi Division
Contak TR Multiprogrammable Pacemaker, DDDR Model 1241 2 05/29/2003 FEI # 2124215
Guidant Corp-Cpi Division
Pulsar Multiprogrammable Pacemaker, DDD Model 970 2 05/29/2003 FEI # 2124215
Guidant Corp-Cpi Division
Pulsar Multiprogrammable Pacemaker, DDD Model 972 2 05/29/2003 FEI # 2124215
Guidant Corp-Cpi Division
Pulsar Multiprogrammable Pacemaker, DDD Model 976 2 05/29/2003 FEI # 2124215
Guidant Corp-Cpi Division
Pulsar Multiprogrammable Pacemaker, DDDR Model 1270 2 05/29/2003 FEI # 2124215
Guidant Corp-Cpi Division
Pulsar Multiprogrammable Pacemaker, DDDR Model 1272 2 05/29/2003 FEI # 2124215
Guidant Corp-Cpi Division
Pulsar Max Multiprogrammable Pacemaker 2 05/29/2003 FEI # 2124215
Guidant Corp-Cpi Division
Pulsar Max II Multiprogrammable Pacemaker, DDDR Model 1284 2 05/29/2003 FEI # 2124215
Guidant Corp-Cpi Division

*   The maximium 500 devices meeting your search criteria returned. Please narrow your search.
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