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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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Z-1748-2022 - SCENARIA View: Software Version V1.08, V1.09B, V1.09C, V1.09D, V1.0B, V1.0C 2 09/16/2022 FUJIFILM Healthcare Americas Corporation
Z-1750-2022 - Surpria 64: Software Version V3.11, V3.22 2 09/16/2022 FUJIFILM Healthcare Americas Corporation
Z-1749-2022 - Surpria: Software Version V3.11, V3.22 2 09/16/2022 FUJIFILM Healthcare Americas Corporation
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