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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 4 of 4 Results
Related Medical Device Recalls
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Product Description
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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... 2 01/18/2011 Stryker Instruments Div. of Stryker Corporation
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... 2 01/18/2011 Stryker Instruments Div. of Stryker Corporation
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 ... 2 01/18/2011 Stryker Instruments Div. of Stryker Corporation
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 ... 2 01/18/2011 Stryker Instruments Div. of Stryker Corporation
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