Medical Device Recalls
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51 to 60 of 284 Results
Product: pacemaker |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Pulsar Multiprogrammable Pacemaker, DDDR Model 1272 | 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 976 | 2 | 05/29/2003 | Guidant Corp-Cpi Division |
Pulsar Multiprogrammable Pacemaker, DDD Model 972 | 2 | 05/29/2003 | Guidant Corp-Cpi Division |
Pulsar Max Multiprogrammable Pacemaker | 2 | 05/29/2003 | Guidant Corp-Cpi Division |
Pulsar Max II Multiprogrammable Pacemaker, Model 1280 | 2 | 07/15/2003 | Guidant Corp-Cpi Division |
Pulsar Max II Multiprogrammable Pacemaker, Model 1181 | 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, 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 |
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