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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 10 of 23 Results
Related Medical Device Recalls
 
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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Z-0875-03 - Pulsar Multiprogrammable Pacemaker, DDD Model 970 2 05/29/2003 Guidant Corp-Cpi Division
Z-0897-03 - Contak TR Multiprogrammable Pacemaker, DDDR Model 1241 2 05/29/2003 Guidant Corp-Cpi Division
Z-0877-03 - Pulsar Multiprogrammable Pacemaker, DDD Model 976 2 05/29/2003 Guidant Corp-Cpi Division
Z-0878-03 - Pulsar Multiprogrammable Pacemaker, DDDR Model 1270 2 05/29/2003 Guidant Corp-Cpi Division
Z-0879-03 - Pulsar Multiprogrammable Pacemaker, DDDR Model 1272 2 05/29/2003 Guidant Corp-Cpi Division
Z-0880-03 - Pulsar Max Multiprogrammable Pacemaker 2 05/29/2003 Guidant Corp-Cpi Division
Z-0881-03 - Pulsar Max II Multiprogrammable Pacemaker, DDDR Model 1284 2 05/29/2003 Guidant Corp-Cpi Division
Z-0882-03 - Pulsar Max II Multiprogrammable Pacemaker, DDDR Model 1286 2 05/29/2003 Guidant Corp-Cpi Division
Z-0883-03 - Discovery Multiprogrammable Pacemaker, DDDR Model 1273 2 05/29/2003 Guidant Corp-Cpi Division
Z-0884-03 - Discovery Multiprogrammable Pacemaker, DDDR Model 1274 2 05/29/2003 Guidant Corp-Cpi Division
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