Medical Device Recalls
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1 result found
Related Medical Device Recalls |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Z-2247-2017 - KYPHON(R) Directional Bone Filler Device, Size: 3, REF F04C, Rx Only, STERILE R. | 2 | 06/03/2017 | Medtronic Sofamor Danek USA Inc |
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