Medical Device Recalls
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1 to 9 of 9 Results
Related Medical Device Recalls |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Z-1009-03 - Pulsar Max II Multiprogrammable Pacemaker, Model 1180 | 2 | 07/15/2003 | Guidant Corp-Cpi Division |
Z-1010-03 - Pulsar Max II Multiprogrammable Pacemaker, Model 1181 | 2 | 07/15/2003 | Guidant Corp-Cpi Division |
Z-1011-03 - Discovery II Multiprogrammable Pacemaker, Model 0481 | 2 | 07/15/2003 | Guidant Corp-Cpi Division |
Z-1012-03 - Discovery II Multiprogrammable Pacemaker, Model 0981 | 2 | 07/15/2003 | Guidant Corp-Cpi Division |
Z-1017-03 - Pulsar Max II Multiprogrammable Pacemaker, Model 1280 | 2 | 07/15/2003 | Guidant Corp-Cpi Division |
Z-1014-03 - Discovery II Multiprogrammable Pacemaker, Model 1283 | 2 | 07/15/2003 | Guidant Corp-Cpi Division |
Z-1015-03 - Discovery II Multiprogrammable Pacemaker, Model 1284 | 2 | 07/15/2003 | Guidant Corp-Cpi Division |
Z-1016-03 - Discovery II Multiprogrammable Pacemaker, Model 1286 | 2 | 07/15/2003 | Guidant Corp-Cpi Division |
Z-1013-03 - Discovery II Multiprogrammable Pacemaker, Model 1184 | 2 | 07/15/2003 | Guidant Corp-Cpi Division |
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