Medical Device Recalls
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1 to 3 of 3 Results
Related Medical Device Recalls |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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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 | 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 | 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 | Pro-Med Instruments Gmbh |
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