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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-0912-2011 - Stryker Instruments, SmartPump Tourniquet System, Dual Channel Tourniquet Pump, REF 5920-011-000, Rx only.
Intended to be used to temporarily occlude or decrease blood flow in a patient extremity dur...
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2
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01/18/2011
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Stryker Instruments Div. of Stryker Corporation
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Z-0915-2011 - Stryker Instruments, Interventional Spine RF MultiGen REF 0406-900-000, Rx only,, Stryker Instruments, Kalamazoo, MI (USA), 49001, (269) 323-7700, (800) 253-3210.
The product is intended for coagulat...
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2
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01/18/2011
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Stryker Instruments Div. of Stryker Corporation
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Z-0914-2011 - Stryker Instruments, SmartPump Tourniquet System, Report Printer Kit, REF 5920-012-000, Rx only, Stryker Instruments, Kalamazoo, MI (USA), 49001, (269) 323-7700, (800) 253-3210.
Provides a record of ...
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2
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01/18/2011
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Stryker Instruments Div. of Stryker Corporation
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Z-0913-2011 - Stryker Instruments, SmartPump Tourniquet System, Single Channel Tourniquet Pump, REF 5920-010-000, Rx only, Stryker Instruments, Kalamazoo, MI (USA), 49001, (269) 323-7700, (800) 253-3210.
Intended ...
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2
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01/18/2011
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Stryker Instruments Div. of Stryker Corporation
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