Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K123754 |
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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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| C10-3v Transducer Probe | 3 | 08/22/2025 |
FEI # 2518586 Philips Ultrasound, Inc |
| C9-3io Transducer Probe | 3 | 08/22/2025 |
FEI # 2518586 Philips Ultrasound, Inc |
| Transducer C10-3v Transducer Probe | 3 | 08/22/2025 |
FEI # 2518586 Philips Ultrasound, Inc |
| L10-4LAP Transducer Probe | 3 | 08/22/2025 |
FEI # 2518586 Philips Ultrasound, Inc |
| eL18-4 Transducer Probe | 3 | 08/22/2025 |
FEI # 2518586 Philips Ultrasound, Inc |
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