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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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FDA Recall
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Z-0435-2021 - OsteoBridge Intremedullary Knee Arthrodesis (IKA) nails 2 11/06/2020 Merete Medical GmbH
Z-0438-2021 - OsteoBridge Intramedullary Diaphysis Segment Fixation (IDSF) nails (humerus) 2 11/06/2020 Merete Medical GmbH
Z-0437-2021 - OsteoBridge Intramedullary Diaphysis Segment Fixation (IDSF) nails (tibia) 2 11/06/2020 Merete Medical GmbH
Z-0436-2021 - OsteoBridge Intramedullary Diaphysis Segment Fixation (IDSF) nails (femur) 2 11/06/2020 Merete Medical GmbH
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