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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 5 of 5 Results
Related Medical Device Recalls
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Product Description
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FDA Recall
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Z-2279-2023 - Field Upgrade Kits: P/N 5451208 RIU, 9 INCH, TOSHIBA; P/N 5485304 SERVICE PART, IMAGE INTENSIFIER, 9 INCH, TOSHIBA; P/N 5761613 SERVICE PART, IMAGE INTENSIFIER, 9 INCH - used with OEC Flexiview 8800, ... 2 07/31/2023 GE OEC Medical Systems, Inc
Z-2276-2023 - OEC 9800 Systems with 9-inch Image Intensifier 2 07/31/2023 GE OEC Medical Systems, Inc
Z-2277-2023 - OEC 9900 Systems with 9-inch Image Intensifier 2 07/31/2023 GE OEC Medical Systems, Inc
Z-2278-2023 - OEC Elite Systems with 9-inch Image Intensifier 2 07/31/2023 GE OEC Medical Systems, Inc
Z-2275-2023 - OEC Flexiview 8800 Systems with 9-inch Image Intensifier 2 07/31/2023 GE OEC Medical Systems, Inc
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