Medical Device Recalls
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1 result found
Recall Number: Z-2170-2026 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Philips Azurion. System Code Description (Model Number): Azurion 3 M12 (722221, 722229), Azurion 3 M... | 2 | 05/12/2026 |
FEI # 3042175844 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. |
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