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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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Class
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FDA Recall
Posting Date
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Z-1192-2008 - Stryker VertePort, 10 G Access Cannula w/Long Stylet System, REF 306-400, Qty 6; For use with the Stryker PCD Precision System and ACM Delivery System, Rx only, sterile, Stryker Instruments, Kalamazoo... 2 03/11/2008 Stryker Instruments Div. of Stryker Corporation
Z-1195-2008 - Stryker VertePort , 11 G Cement Cannula, REF 306-510 , Qty 18; For use with the Stryker PCD Precision System and ACM Delivery System, Rx only, sterile, Stryker Instruments, Kalamazoo, MI. 2 03/11/2008 Stryker Instruments Div. of Stryker Corporation
Z-1194-2008 - Stryker VertePort, 10 G Access Canula (short), REF 306-430, Qty 6; For use with the Stryker PCD Precision System and ACM Delivery System, Rx only, sterile, Stryker Instruments, Kalamazoo, MI. 2 03/11/2008 Stryker Instruments Div. of Stryker Corporation
Z-1193-2008 - Stryker VertePort, 10 G Cement Cannula, REF 306-410, Qty 18; For use with the Stryker PCD Precision System and ACM Delivery System, Rx only, sterile, Stryker Instruments, Kalamazoo, MI. 2 03/11/2008 Stryker Instruments Div. of Stryker Corporation
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