Medical Device Recalls
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1 result found
Recall Number: Z-0846-2025 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Stryker Blueprint Mixed Reality BP MxR Glenoid Pin Guide, REF MRUE200. Indicated for use during T... | 2 | 01/10/2025 |
FEI # 3000931034 Tornier S.A.S. |
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