Medical Device Recalls
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1 result found
Recall Number: Z-1738-2025 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Blueprint Software, BPUE001. Intended for use by surgeons as a pre surgical planner for shoulder re... | 2 | 05/08/2025 |
FEI # 3000931034 Tornier S.A.S. |
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