Medical Device Recalls
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11 to 14 of 14 Results
510(K) Number: K183063 |
Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Product Name: SmartPath to dStream for 1.5T; Model Numbers: (1) 781260, (2) 782112, (3) 782146 | 2 | 05/16/2025 | Philips North America Llc |
| Product Name: SmartPath to dStream for 3.0T; Model Number: 782145 | 2 | 05/16/2025 | Philips North America Llc |
| Product Name: SmartPath to dStream for XR and 3.0T; Model Numbers: (1) 781270, (2) 782113; | 2 | 05/16/2025 | Philips North America Llc |
| Product Name: SmartPath to Ingenia Elition X; Model Numbers: (1) 782118, (2) 782144; | 2 | 05/16/2025 | Philips North America Llc |
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