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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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Z-1863-2009 - Stryker 550 mL AutoFuser PainPump, single site continuous with bolus, 6 mL/hr, sterile, REF 0535-600-000.
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2
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09/04/2009
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Stryker Instruments Div. of Stryker Corporation
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Z-1864-2009 - Stryker 550 mL AutoFuser PainPump, single site continuous with bolus, 6 mL/hr, 2 mL bolus, sterile, REF 0535-626-000.
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2
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09/04/2009
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Stryker Instruments Div. of Stryker Corporation
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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.
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2
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09/04/2009
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Stryker Instruments Div. of Stryker Corporation
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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.
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2
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09/04/2009
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Stryker Instruments Div. of Stryker Corporation
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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.
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2
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09/04/2009
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Stryker Instruments Div. of Stryker Corporation
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Z-1824-2009 - Stryker 100 mL AutoFuser PainPump, single site continuous, 2.0 mL/hr, sterile, REF 0531-200-000.
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2
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09/04/2009
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Stryker Instruments Div. of Stryker Corporation
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