Medical Device Recalls
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1 result found
Recall Number: Z-2976-2026 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Beckman Coulter, Emit 2000 Quinidine Assay REF: OSR4Q229 Contents: R1: 2 x 23 mL;R2 2x13 mL | 2 | 08/17/2026 |
FEI # 1219913 Siemens Healthcare Diagnostics, Inc. |
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