Medical Device Recalls
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1 result found
Recall Number: Z-0771-2025 |
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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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| SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps used with PROG CT900B CLINI... | 2 | 12/27/2024 |
FEI # 2182207 Medtronic Neuromodulation |
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