Medical Device Recalls
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1 result found
Recall Number: Z-1306-2026 |
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Product Description
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Recall
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FDA Recall
Posting Date |
Recalling Firm
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| Product Name: Lumipulse G ®-Amyloid 1-42-N Plasma Calibrators Model/Catalog Number: 235454 Softwar... | 2 | 02/05/2026 |
FEI # 2521625 Fujirebio Diagnostics, Inc. |
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