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U.S. Department of Health and Human Services

Medical Device Recalls
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Related Medical Device Recalls
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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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Z-0190-2022 - Arietta 850 Ultrasound- Software Version: V1.0.0 through V4.1.3 2 11/02/2021 FujiFilm Healthcare Americas Corporation
Z-0189-2022 - Arietta 750 Ultrasound Software Version: V1.0.0 through V2.1.3 2 11/02/2021 FujiFilm Healthcare Americas Corporation
Z-0191-2022 - Lisendo 880 Ultrasound Software Version: V1.0 through V4.1.3 2 11/02/2021 FujiFilm Healthcare Americas Corporation
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