Medical Device Recalls
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1 result found
Recall Number: Z-0708-2025 |
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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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| Monitoring Service Application (MSA). Software to process, analyze, display, and report cardiac even... | 1 | 12/23/2024 |
FEI # 3003584029 Braemar Manufacturing, LLC |
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