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U.S. Department of Health and Human Services

Medical Device Recalls

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251 to 260 of 284 Results
Product: pacemaker
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Product Description
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Recall
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FDA Recall
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Discovery II Multiprogrammable Pacemaker, Model 1284 2 07/15/2003 Guidant Corp-Cpi Division
Pulsar Max II Multiprogrammable Pacemaker, Model 1180 2 07/15/2003 Guidant Corp-Cpi Division
Pulsar Max II Multiprogrammable Pacemaker, Model 1280 2 07/15/2003 Guidant Corp-Cpi Division
Discovery II Multiprogrammable Pacemaker, Model 1286 2 07/15/2003 Guidant Corp-Cpi Division
Pulsar Max II Multiprogrammable Pacemaker, Model 1181 2 07/15/2003 Guidant Corp-Cpi Division
Insignia Plus Multiprogrammable Pacemaker, DDD Model 986 2 05/29/2003 Guidant Corp-Cpi Division
Insignia Plus Multiprogrammable Pacemaker, DDDR Model 1294 2 05/29/2003 Guidant Corp-Cpi Division
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
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