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U.S. Department of Health and Human Services

Medical Device Recalls

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11 to 18 of 18 Results
Related Medical Device Recalls
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Product Description
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Class
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FDA Recall
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Z-0877-2016 - Stryker, T2 Guidewire, Ball-Tipped, 2.5 x 1000mm Product Usage: Intended for the temporary stabilization of bone segments or fragments. 2 02/25/2016 Stryker Howmedica Osteonics Corp.
Z-0878-2016 - Stryker, T2 Guidewire, Ball-Tipped, 3 x 1000mm Product Usage: Intended for the temporary stabilization of bone segments or fragments. 2 02/25/2016 Stryker Howmedica Osteonics Corp.
Z-0879-2016 - Stryker, T2 Guidewire, Smooth-Tipped, 3 x 800mm Product Usage: Intended for the temporary stabilization of bone segments or fragments. 2 02/25/2016 Stryker Howmedica Osteonics Corp.
Z-0880-2016 - Stryker, T2 Guidewire, Smooth-Tipped, 2.2 x 800mm Product Usage: Intended for the temporary stabilization of bone segments or fragments. 2 02/25/2016 Stryker Howmedica Osteonics Corp.
Z-0881-2016 - Stryker, T2 Guidewire, Ball Tipped, 3 x 1250mm Product Usage: Intended for the temporary stabilization of bone segments or fragments. 2 02/25/2016 Stryker Howmedica Osteonics Corp.
Z-0882-2016 - Stryker, T2 Fixation K-Wire 3 x 285mm WCH coated Product Usage: Intended for the temporary stabilization of bone segments or fragments. 2 02/25/2016 Stryker Howmedica Osteonics Corp.
Z-0883-2016 - Stryker, T2 K-Wire, 3.2x400mm, Recon Product Usage: Intended for the temporary stabilization of bone segments or fragments. 2 02/25/2016 Stryker Howmedica Osteonics Corp.
Z-0868-2016 - Stryker, METAIZEAU Intramedullary Pin, 2.0 x 400 mm Product Usage: Intended for the temporary stabilization of bone segments or fragments. 2 02/25/2016 Stryker Howmedica Osteonics Corp.
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