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U.S. Department of Health and Human Services

Medical Device Recalls
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Related Medical Device Recalls
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Z-0352-2018 - Medtronic KYPHON(R) Express(TM) Directional Bone Filler Device, SIZE 2, REF FB, QTY 1 EA, Rx only STERILE R 2 01/14/2018 FEI # 1000477302
Medtronic Sofamor Danek USA Inc
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