Discovery 670 DR (UDI 00840682124393)Recalls & reported problems
G E Medical Systems Israel Ltd. · Class 2
All models of Discovery (4)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 2
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
2 FDA recall records name this device's identifier, 1 still open.
20 other recalls cover devices cleared under the same FDA submission (K093514); they may or may not involve this specific model.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Recalls naming this device
- Dec 18, 2024Open, Classified
GE HealthCare has become aware that certain Infinia, VariCam/VG/VH, Brivo NM 615, Discovery NM 630, Discovery NM/CT 670, and Optima NM/CT 640 Nuclear Medicine systems (see Affected Products Details and Appendices) could have been transported or relocated without proper detector support, which can result in excessive load being applied to the detector mounting mechanisms. If this occurs, it can potentially result in a detector fall and lead to life-threatening bodily injury.
Z-0892-2025 · Root cause: Package design/selection · Recall details · FDA record ↗
- May 24, 2018Completed
When your system was installed, the Main disconnect switch, EPO button on the A1 panel, and Remote EPO button(s) (outside of the A1 panel) may not have been wired correctly which could result in these not shutting off all power to the entire system as intended, resulting in a potential electric hazard.
Z-0606-2019 · Root cause: Component change control · Recall details · FDA record ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K093514. One submission often covers many models, so check the product and lot details in each record.
- Z-0894-2025 · Dec 18, 2024 · Open, ClassifiedGE Healthcare Discovery NM/CT 670 ES, Model/Catalog Numbers: 1) H3100XF ; System, Tomography, Computed, Emission
- Z-0893-2025 · Dec 18, 2024 · Open, ClassifiedGE Healthcare Discovery NM/CT 670 PRO, Model/Catalog Numbers: 1) 5376204-70-54-2; 2) H2401AK; 3) H2402AC; 4) H3100AH; 5) H3100XB; System, Tomography, Computed, Emission
- Z-0891-2025 · Dec 18, 2024 · Open, ClassifiedGE Healthcare Discovery NM/CT 670, Model/Catalog Numbers: 1) 5376204-70-54-2, 2) H2401BC, 3) H2401CE, 4) H2401CG, 5) H3100AG, 6) H3100JW, 7) H3100NC; System, Tomography, Co
- Z-0895-2025 · Dec 18, 2024 · Open, ClassifiedGE Healthcare Discovery NM/CT 670 CZT, Model/Catalog Numbers: 1) H3906AB; System, Tomography, Computed, Emission
- Z-1053-2023 · Dec 19, 2022 · Open, ClassifiedGE Nuclear Medicine 600/800 series systems, specifically: a) 870, b) 870 DR 3/8 inch NM GANTRY WITH NEW ROTOR - MEA, c) 870 DR / Dismount, d) 870 DR / Dismount / 60HZ, e) 870
- Z-1547-2021 · Feb 7, 2021 · Open, ClassifiedNM/CT 870 DR Nuclear Medicine / CT Scanners
- Z-0857-2021 · Dec 10, 2020 · TerminatedDiscovery 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
- Z-2997-2020 · Aug 14, 2020 · TerminatedDiscovery NM670 Pro Model # H3100XB
- Z-2996-2020 · Aug 14, 2020 · TerminatedDiscovery 670 DR Model # H3100BT
- Z-2998-2020 · Aug 14, 2020 · TerminatedNM/CT 870 DR Model # H3100AS
- Z-1260-2019 · Mar 20, 2019 · TerminatedDiscovery NM/CT 670 ES Product Usage: The GE Discovery NM/CT 670 system is a medical tool intended for use by appropriately trained health professionals to aid in detecting, local
- Z-1259-2019 · Mar 20, 2019 · TerminatedDiscovery NM/CT 670 DR Product Usage: The GE Discovery NM/CT 670 system is a medical tool intended for use by appropriately trained health professionals to aid in detecting, loca
- Z-1265-2019 · Mar 20, 2019 · TerminatedNM/CT 870 DR Product Usage: The GE Discovery NM/CT 670 system is a medical tool intended for use by appropriately trained health professionals to aid in detecting, localizing, di
- Z-0607-2019 · May 24, 2018 · CompletedDiscovery NM/CT 670 ES, model 5376204-70-57
- Z-0608-2019 · May 24, 2018 · CompletedDiscovery NM/CT 670 Pro, model 5376204-70-54
…and 5 more.
Other System, x-ray, tomography, computed devices
- ARTIS icono biplane 11327600Siemens Healthcare GmbH · System, x-ray, tomography, computed15 recalls2 deaths55 reports
- ARTIS icono floor 11327700Siemens Healthcare GmbH · System, x-ray, tomography, computed15 recalls24 reports
- Incisive CTPhilips Healthcare (Suzhou) Co., Ltd. · System, x-ray, tomography, computed13 recalls5 reports
- Spectral CTPhilips Medical Systems Nederland B.V. · System, x-ray, tomography, computed11 recalls3 reports
- Incisive CTPhilips Healthcare (Suzhou) Co., Ltd. · System, X-Ray, Tomography, Computed9 recalls20 reports
- Brilliance iCTPhilips Medical Systems Nederland B.V. · System, x-ray, tomography, computed8 recalls6 reports
- Revolution Apex EliteGE Medical Systems, L.L.C. · System, x-ray, tomography, computed8 recalls0 reports
- Brilliance CT Big BorePhilips Medical Systems Nederland B.V. · System, x-ray, tomography, computed7 recalls1 report
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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