Medical Device Recalls
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1 result found
Recall Number: Z-2503-2025 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Philips Allura System configured with a 1 Phase UPS. Allura family (R1.x, R2.x). Labeled as the ... | 2 | 09/03/2025 |
FEI # 3002807880 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. |
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