Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K231190 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| mL26-8 Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
| Philips EPIQ Diagnostic Ultrasound System Models: EPIQ 7G(model # 795200), EPIQ 7C (Model # 795201)... | 2 | 11/09/2023 | Philips Ultrasound, Inc. |
| Philips Affiniti 70, Diagnostic Ultrasound System Model # 795210 | 2 | 11/09/2023 | Philips Ultrasound, Inc. |
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