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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 12 Results
510(K) Number: K042405
 
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Stryker PainPump Two Site Infusion Kit with ExFen 5.0", 120 mL Infusion Kit, sterile, 5 per box. Ma... 2 02/02/2009 FEI # 1811755
Stryker Instruments Div. of Stryker Corporation
Stryker PainPump, Two Site Infusion Kit with ExFen 2.5", 120 mL Infusion Kit, sterile, 5 per box. M... 2 02/02/2009 FEI # 1811755
Stryker Instruments Div. of Stryker Corporation
Stryker PainPump Two Site Infusion Set, sterile, 10 per box. Manufactured for Stryker Instruments, K... 2 02/02/2009 FEI # 1811755
Stryker Instruments Div. of Stryker Corporation
Stryker PainPump1 1-Day Infusion Kit; Product number 500-140-000. 2 03/21/2006 FEI # 1811755
Stryker Instruments Div. of Stryker Corporation
Stryker PainPump1 2-Site Y-Connector; Product number 500-200-000. 2 03/21/2006 FEI # 1811755
Stryker Instruments Div. of Stryker Corporation
Stryker PainPump1.5 Base Infusion Kit; Product number 501-100-000. 2 03/21/2006 FEI # 1811755
Stryker Instruments Div. of Stryker Corporation
Stryker PainPump1.5 5-Day Infusion Kit; Product number 501-120-000. 2 03/21/2006 FEI # 1811755
Stryker Instruments Div. of Stryker Corporation
Stryker PainPump1.5 2-Day Infusion Kit; Product number 501-140-000. 2 03/21/2006 FEI # 1811755
Stryker Instruments Div. of Stryker Corporation
Stryker PainPump1 2-Day Infusion Kit; Product number 500-120-000. 2 03/21/2006 FEI # 1811755
Stryker Instruments Div. of Stryker Corporation
Stryker PainPump1 5-Day Infusion Kit ; Product number 500-110-000. 2 03/21/2006 FEI # 1811755
Stryker Instruments Div. of Stryker Corporation
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