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U.S. Department of Health and Human Services

Medical Device Recalls

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111 to 120 of 279 Results
Product: pacemaker
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Product Description
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FDA Recall
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Insignia Plus Multiprogrammable Pacemaker, DDDR Model 1295 2 05/29/2003 Guidant Corp-Cpi Division
Insignia Entra Multiprogrammable Pacemaker, DDDR Model 1296 2 05/29/2003 Guidant Corp-Cpi Division
Insignia Entra Multiprogrammable Pacemaker, DDDR Model 1297 2 05/29/2003 Guidant Corp-Cpi Division
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
Discovery Multiprogrammable Pacemaker, DDDR Model 1274 2 05/29/2003 Guidant Corp-Cpi Division
Discovery Multiprogrammable Pacemaker, DDDR Model 1273 2 05/29/2003 Guidant Corp-Cpi Division
Pulsar Max II Multiprogrammable Pacemaker, DDDR Model 1286 2 05/29/2003 Guidant Corp-Cpi Division
Pulsar Max II Multiprogrammable Pacemaker, DDDR Model 1284 2 05/29/2003 Guidant Corp-Cpi Division
Pulsar Max Multiprogrammable Pacemaker 2 05/29/2003 Guidant Corp-Cpi Division
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