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U.S. Department of Health and Human Services

Medical Device Recalls
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21 to 23 of 23 Results
Related Medical Device Recalls
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Product Description
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Recall
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FDA Recall
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Recalling Firm
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Z-0875-03 - Pulsar Multiprogrammable Pacemaker, DDD Model 970 2 05/29/2003 FEI # 2124215
Guidant Corp-Cpi Division
Z-0879-03 - Pulsar Multiprogrammable Pacemaker, DDDR Model 1272 2 05/29/2003 FEI # 2124215
Guidant Corp-Cpi Division
Z-0878-03 - Pulsar Multiprogrammable Pacemaker, DDDR Model 1270 2 05/29/2003 FEI # 2124215
Guidant Corp-Cpi Division
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