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U.S. Department of Health and Human Services

Medical Device Recalls
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491 to 500 of 500 Results *
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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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Pulsar Max II Multiprogrammable Pacemaker, DDDR Model 1286 2 05/29/2003 FEI # 2124215
Guidant Corp-Cpi Division
Discovery Multiprogrammable Pacemaker, DDDR Model 1273 2 05/29/2003 FEI # 2124215
Guidant Corp-Cpi Division
Discovery Multiprogrammable Pacemaker, DDDR Model 1274 2 05/29/2003 FEI # 2124215
Guidant Corp-Cpi Division
Discovery II Multiprogrammable Pacemaker, DDD Model 981 2 05/29/2003 FEI # 2124215
Guidant Corp-Cpi Division
Discovery II Multiprogrammable Pacemaker, DDDR Model 1280 2 05/29/2003 FEI # 2124215
Guidant Corp-Cpi Division
Discovery II Multiprogrammable Pacemaker, DDDR Model 1283 2 05/29/2003 FEI # 2124215
Guidant Corp-Cpi Division
Meridian Multiprogrammable Pacemaker, DDDR Model 1275 2 05/29/2003 FEI # 2124215
Guidant Corp-Cpi Division
Meridian Multiprogrammable Pacemaker, DDDR Model 1276 2 05/29/2003 FEI # 2124215
Guidant Corp-Cpi Division
Trident Insert Impactor 2 05/29/2003 FEI # 3003070421
Stryker Howmedica Osteonics
ACCESS Estradiol Reagent Test System 3 05/29/2003 FEI # 2050012
Beckman Coulter Inc

*   The maximium 500 devices meeting your search criteria returned. Please narrow your search.
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