Medical Device Recalls
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1 to 7 of 7 Results
510(K) Number: K172607 |
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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| Philips S8-3t Transducer. | 2 | 07/02/2025 |
FEI # 2518586 Philips Ultrasound, Inc |
| Philips XL14-3 Transducer. | 2 | 07/02/2025 |
FEI # 2518586 Philips Ultrasound, Inc |
| Philips eL18-4 EMT Transducer. | 2 | 07/02/2025 |
FEI # 2518586 Philips Ultrasound, Inc |
| Philips eL18-4 Transducer. | 2 | 07/02/2025 |
FEI # 2518586 Philips Ultrasound, Inc |
| S8-3t Transducer Probe | 3 | 08/22/2025 |
FEI # 2518586 Philips Ultrasound, Inc |
| Transducer S8-3t UDI (01)00884838073524 REF 989605431171 Can be used as accessory with: EPIQ ... | 2 | 05/01/2020 |
FEI # 3019216 Philips Ultrasound Inc |
| XL14-3 Transducer Probe | 3 | 08/22/2025 |
FEI # 2518586 Philips Ultrasound, Inc |
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