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U.S. Department of Health and Human Services

Medical Device Recalls
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41 to 46 of 46 Results
Related Medical Device Recalls Recall Date to: 09/02/2015
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Product Description
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Z-1863-2009 - Stryker 550 mL AutoFuser PainPump, single site continuous with bolus, 6 mL/hr, sterile, REF 0535-600-000. 2 09/04/2009 Stryker Instruments Div. of Stryker Corporation
Z-1864-2009 - Stryker 550 mL AutoFuser PainPump, single site continuous with bolus, 6 mL/hr, 2 mL bolus, sterile, REF 0535-626-000. 2 09/04/2009 Stryker Instruments Div. of Stryker Corporation
Z-1865-2009 - Stryker 550 mL AutoFuser PainPump, single site continuous with bolus, 6 mL/hr, 2 mL bolus, 60 minute bolus refill, 1 x 10.0 in. catheter, sterile, REF 0535-626-010. 2 09/04/2009 Stryker Instruments Div. of Stryker Corporation
Z-1866-2009 - Stryker 550 mL AutoFuser PainPump, single site continuous with bolus, 6 mL/hr, 2 mL bolus, 60 minute bolus refill, 1 x 2.5 in. catheter, sterile, REF 0535-626-025. 2 09/04/2009 Stryker Instruments Div. of Stryker Corporation
Z-1867-2009 - Stryker 550 mL AutoFuser PainPump, single site continuous with bolus, 6 mL/hr, 2 mL bolus, 60 minute bolus refill, 1 x 5.0 in. catheter, sterile, REF 0535-626-050. 2 09/04/2009 Stryker Instruments Div. of Stryker Corporation
Z-1824-2009 - Stryker 100 mL AutoFuser PainPump, single site continuous, 2.0 mL/hr, sterile, REF 0531-200-000. 2 09/04/2009 Stryker Instruments Div. of Stryker Corporation
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