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U.S. Department of Health and Human Services

Medical Device Recalls

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Related Medical Device Recalls Recall Date to: 07/02/2015
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Product Description
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FDA Recall
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Z-0010-2008 - EPIK® KNEE SYSTEM Angled Insert Impactor RM/LL; Part #801-03-052 Rev. A; non-sterile; knee prosthesis instrument. Distributed by Encore Medical, L.P., Austin, TX 78758. 2 10/10/2007 Encore Medical, Lp
Z-0009-2008 - EPIK® KNEE SYSTEM Angled Insert Impactor LM/RL; Catalog #801-03-051 Rev. A; non-sterile; knee prosthesis instrument. Distributed by Encore Medical, L.P., Austin, TX 78758. 2 10/10/2007 Encore Medical, Lp
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