Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K062247 |
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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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| C6-3 Transducer Probe | 3 | 08/22/2025 |
FEI # 2518586 Philips Ultrasound, Inc |
| Philips V6-2 Transducer. | 2 | 07/02/2025 |
FEI # 2518586 Philips Ultrasound, Inc |
| V6-2 Transducer Probe | 3 | 08/22/2025 |
FEI # 2518586 Philips Ultrasound, Inc |
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