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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 6 of 6 Results
Related Medical Device Recalls
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Z-0857-2021 - Discovery 670 DR (Model H3100BT), NM/CT 870 DR (Model 3100Q and H3100AS), Discovery NM670 Pro (Model 3100XB), Discovery 670 ES (Model H3100XF) - Product Usage: intended for use by appropriately traine... 2 01/13/2021 FEI # 2126677
GE Healthcare, LLC
Z-0856-2021 - Discovery NM 630 (Model Number H3101RH), NM 830 (Model Number H3910AC), 830 NM Cyber Defense (Model Number H3910AG) - Product Usage: intended for general Nuclear Medicine imaging procedures for detect... 2 01/13/2021 FEI # 2126677
GE Healthcare, LLC
Z-0853-2021 - GE NM/CT 850 system Model Number H3907AD - Product Usage: intended for general Nuclear Medicine imaging procedures for detection of radioisotope tracer uptake in the patient body. 2 01/13/2021 FEI # 2126677
GE Healthcare, LLC
Z-0854-2021 - GE NM/CT 860 system Model Number H3908AD - Product Usage: intended for general Nuclear Medicine imaging procedures for detection of radioisotope tracer uptake in the patient body. 2 01/13/2021 FEI # 2126677
GE Healthcare, LLC
Z-0855-2021 - GE NM/CT 870 CZT system Model Number H3906CW - Product Usage: intended for general Nuclear Medicine imaging procedures for detection of radioisotope tracer uptake in the patient body. 2 01/13/2021 FEI # 2126677
GE Healthcare, LLC
Z-0858-2021 - Optima NM/CT 640, Model number 3101RL - Product Usage: intended for General Nuclear Medicine imaging procedures for detection of radioisotope tracer uptake in the patient body. 2 01/13/2021 FEI # 2126677
GE Healthcare, LLC
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