Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K152899 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| C5-2 Lumify Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
| L12-4 Lumify Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
| L12-4 Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
| Philips Lumify Diagnostic Ultrasound, Catalogue Number: 795216 Part Number: 989605449841 with 45356... | 2 | 01/06/2016 | Philips Ultrasound, Inc. |
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