Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K212813 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Zenition 70. The device is to be used in health care facilities both inside and outside the operatin... | 2 | 04/21/2025 | Philips Medical Systems Nederland B.V. |
| Zenition 70. Product Code 718133. The devices are used for radiological guidance and visualization d... | 2 | 04/21/2025 | Philips North America Llc |
| Philips Zenition 70, Model Number: 718133 | 2 | 11/12/2024 | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. |
| Zenition 50 & 70 Mobile Surgery C-arm | 2 | 09/30/2024 | Philips North America |
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