Medical Device Recalls
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1 result found
Recall Number: Z-0032-2026 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| DxC 500 AU Module w/ISE, DxC 500i, With ISE, REF: C63522 and DxC 500 AU Module, DxC 500i, Without IS... | 2 | 10/02/2025 |
FEI # 2050012 Beckman Coulter Inc. |
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