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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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FDA Recall
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Z-2578-2018 - Discovery IQ 2.0 20cm, 4 ring, Model Number 5432539-22 2 07/31/2018 GE Healthcare, LLC
Z-2579-2018 - Discovery MI Digital Ready 2 07/31/2018 GE Healthcare, LLC
Z-2580-2018 - Discovery MI, labeled as Discovery DMI 15 cm 3 ring, and Discovery DMI 20cm 4 ring 2 07/31/2018 GE Healthcare, LLC
Z-2581-2018 - Discovery RT labeled as: a. MID BJG; b. HVY BJG 2 07/31/2018 GE Healthcare, LLC
Z-2587-2018 - CT Goldseal BrightSpeed 16 PWR TIO 2 YR 2 07/31/2018 GE Healthcare, LLC
Z-2583-2018 - CT Goldseal Optima CT 600 2 07/31/2018 GE Healthcare, LLC
Z-2584-2018 - Revolution EVO 3.6, labeled as a. HVY WAUK; b. LONG HINO; c. LONG WAUK; d. MID BJG; e. MID WAUK. 2 07/31/2018 GE Healthcare, LLC
Z-2585-2018 - Optima CT 520 2 07/31/2018 GE Healthcare, LLC
Z-2586-2018 - Optima CT 540 2 07/31/2018 GE Healthcare, LLC
Z-2582-2018 - Revolution CT 160 1.5D STD WAUK 2 07/31/2018 GE Healthcare, LLC
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