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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 9 of 9 Results
Related Medical Device Recalls
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Product Description
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FDA Recall
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Z-0668-06 - Stryker PainPump1.5 Base Infusion Kit; Product number 501-100-000. 2 03/21/2006 Stryker Instruments Div. of Stryker Corporation
Z-0669-06 - Stryker PainPump1.5 5-Day Infusion Kit; Product number 501-120-000. 2 03/21/2006 Stryker Instruments Div. of Stryker Corporation
Z-0670-06 - Stryker PainPump1.5 2-Day Infusion Kit; Product number 501-140-000. 2 03/21/2006 Stryker Instruments Div. of Stryker Corporation
Z-0662-06 - Stryker PainPump1 Base Kit; Product number 500-100-000. 2 03/21/2006 Stryker Instruments Div. of Stryker Corporation
Z-0663-06 - Stryker PainPump1 5-Day Infusion Kit ; Product number 500-110-000. 2 03/21/2006 Stryker Instruments Div. of Stryker Corporation
Z-0667-06 - Stryker PainPump1 2-Site Y-Connector; Product number 500-250-000. 2 03/21/2006 Stryker Instruments Div. of Stryker Corporation
Z-0666-06 - Stryker PainPump1 2-Site Y-Connector; Product number 500-200-000. 2 03/21/2006 Stryker Instruments Div. of Stryker Corporation
Z-0664-06 - Stryker PainPump1 2-Day Infusion Kit; Product number 500-120-000. 2 03/21/2006 Stryker Instruments Div. of Stryker Corporation
Z-0665-06 - Stryker PainPump1 1-Day Infusion Kit; Product number 500-140-000. 2 03/21/2006 Stryker Instruments Div. of Stryker Corporation
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