Medical Device Recalls
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1 to 10 of 21 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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| D5cwc Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
| Transducer C10-3v Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
| S8-3 Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
| S12-4 Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
| C10-3v Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
| c5-1 Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
| C8-5 Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
| C9-3io Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
| C9-3v Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
| D2cwc Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
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