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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| 3D9-3v Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
| BP10-5ec Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
| C10-3v Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
| C10-4ec Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
| C6-2 Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
| C9-2 Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
| C9-4v Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
| D2TCD Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
| L18-5 Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
| Mini Multi TEE Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
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