Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K162583 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Lisendo 880 Ultrasound Software Version: V1.0 through V4.1.3 | 2 | 11/02/2021 | FujiFilm Healthcare Americas Corporation |
| UST-2265-2 Probe, Part Number: UST-2265-2 - Product Usage: The UST-2265-2 probe is intended to be us... | 2 | 02/20/2020 | Hitachi Medical Systems America Inc |
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