Medical Device Recalls
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161 to 170 of 284 Results
Product: pacemaker |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Discovery II Multiprogrammable Pacemaker, Model 1284 | 2 | 07/15/2003 | Guidant Corp-Cpi Division |
Discovery II Multiprogrammable Pacemaker, Model 1283 | 2 | 07/15/2003 | Guidant Corp-Cpi Division |
Discovery II Multiprogrammable Pacemaker, Model 1184 | 2 | 07/15/2003 | Guidant Corp-Cpi Division |
Discovery II Multiprogrammable Pacemaker, Model 0981 | 2 | 07/15/2003 | Guidant Corp-Cpi Division |
Discovery II Multiprogrammable Pacemaker, Model 0481 | 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 |
Discovery Multiprogrammable Pacemaker, DDDR Model 1274 | 2 | 05/29/2003 | Guidant Corp-Cpi Division |
Pulsar Multiprogrammable Pacemaker, DDD Model 970 | 2 | 05/29/2003 | Guidant Corp-Cpi Division |
Discovery II Multiprogrammable Pacemaker, DDDR Model 1280 | 2 | 05/29/2003 | Guidant Corp-Cpi Division |
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