Medical Device Recalls
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1 result found
Recall Number: Z-0323-2024 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| DBX Demineralized Bone Matrix Putty 10cc-Indicated for treatment of surgically created osseous defec... | 2 | 11/17/2023 |
FEI # 3001236616 Musculoskeletal Transplant Foundation, Inc. |
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