Medical Device Recalls
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1 to 9 of 9 Results
510(K) Number: K153480 |
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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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| Philips L12-4 Transducer. | 2 | 07/02/2025 | Philips Ultrasound, Inc |
| Philips 3D9-3v Transducer. | 2 | 07/02/2025 | Philips Ultrasound, Inc |
| Philips V6-2 Transducer. | 2 | 07/02/2025 | Philips Ultrasound, Inc |
| L12-5 38mm Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
| S4-1 Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
| L12-4 Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
| V6-2 Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
| 3D9-3v Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
| C9-4v Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
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