Medical Device Recalls
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510(K) Number: K132304 |
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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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| C10-3v 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 |
| V6-2 Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
| TRANSDUCER L12-5 Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
| S8-3 Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
| S7-3t Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
| S12-4 Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
| Mini Multi TEE Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
| L18-5 Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
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