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U.S. Department of Health and Human Services

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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Prot®g® Self-Expanding Nitinol Stent 6 mm x 40 mm, Model Number SER6-6-40-135 3 05/22/2003 FEI # 2183870
ev3, Inc.
STA-Compact Hemostasis System with Cap piercing capability. 2 05/29/2003 FEI # 2245451
Diagnostica Stago, Inc.
Hill-Rom brand Affinity three birthing bed 2 05/29/2003 FEI # 1824206
Hill-Rom, Inc.
Hill-Rom brand Century+ series bed 2 05/29/2003 FEI # 1824206
Hill-Rom, Inc.
Tecan Genesis RSP and NPS Instruments with barcode scanner type PosID2 option with firmware version... 2 05/29/2003 FEI # 1037985
Tecan U S Inc
Insignia Plus Multiprogrammable Pacemaker, DDD Model 985 2 05/29/2003 FEI # 2124215
Guidant Corp-Cpi Division
Insignia Plus Multiprogrammable Pacemaker, DDD Model 986 2 05/29/2003 FEI # 2124215
Guidant Corp-Cpi Division
Insignia Plus Multiprogrammable Pacemaker, DDDR Model 1294 2 05/29/2003 FEI # 2124215
Guidant Corp-Cpi Division
Insignia Plus Multiprogrammable Pacemaker, DDDR Model 1295 2 05/29/2003 FEI # 2124215
Guidant Corp-Cpi Division
Insignia Entra Multiprogrammable Pacemaker, DDDR Model 1296 2 05/29/2003 FEI # 2124215
Guidant Corp-Cpi Division

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