Medical Device Recalls
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1 result found
Recall Number: Z-1661-2026 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| ALLURA Xper FD10; System Code: (1) 722003, (2)722010, (3)722026; | 2 | 03/27/2026 |
FEI # 3042175844 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. |
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