Medical Device Recalls
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510(K) Number: K030455 |
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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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| C5-2 Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
| C8-4v Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
| C8-4v Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
| C8-5 Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
| C9-4 Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
| C9-5ec Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
| D2TCD Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
| D2cwc Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
| D5cwc Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
| L11-3 Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
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