Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K163120 |
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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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| X8-2t Transducer Probe | 3 | 08/22/2025 |
FEI # 2518586 Philips Ultrasound, Inc |
| Philips X8-2t Transducer. | 2 | 07/02/2025 |
FEI # 2518586 Philips Ultrasound, Inc |
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