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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-2970-2018 - DORO LUCENT Base Unit, REF 1101.021 Headrest System used in open and percutaneous craniotomies and spinal surgeries 1 09/17/2018 FEI # 3003923584
Pro-Med Instruments Gmbh
Z-2972-2018 - DORO LUCENT Transitional Member, REF 1101.026 Component of headrest system used in open and percutaneous craniotomies and spinal surgeries 1 09/17/2018 FEI # 3003923584
Pro-Med Instruments Gmbh
Z-2971-2018 - DORO LUCENT Locking Transitional Member, REF 1101.031 Component of headrest system used in open and percutaneous craniotomies and spinal surgeries 1 09/17/2018 FEI # 3003923584
Pro-Med Instruments Gmbh
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