Medical Device Recalls
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510(K) Number: K163120 |
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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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| 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 |
| TRANSDUCER L12-5 Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
| S7-3t Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
| S4-2 Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
| S12-4 Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
| Philips X8-2t Transducer. | 2 | 07/02/2025 | Philips Ultrasound, Inc |
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