Medical Device Recalls
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1 result found
Recall Number: Z-1506-2025 |
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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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| A820 myPTM Software Application associated with Medtronic SynchroMed Pump and Infusion System. | 2 | 04/01/2025 |
FEI # 2182207 Medtronic Neuromodulation |
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