Medical Device Recalls
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1 result found
Related Medical Device Recalls |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Z-2279-2026 - CASE v7.0 Cardiac Testing System Model no. 3031234-001 Product Code SU3 | 2 | 06/01/2026 |
FEI # 3012359877 GE Medical Systems Information Technologies Inc |
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