Medical Device Recalls
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510(K) Number: K181485 |
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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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| C9-2 Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
| X8-2t Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
| X7-2 Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
| X6-1 Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
| X5-1 Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
| VL13-5 Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
| S9-2 Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
| S8-3t Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
| BP10-5ec Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
| C10-4ec Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
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