Official recall record
GE Healthcare Discovery NM/CT 670 CZT, Model/Catalog Numbers: 1) H3906AB; System, Tomography, Computed, Emission
- Issuing authority
- US FDA — Medical Devices
- Alert date
- 2024-12-18
- Country of alert
- Israel
- Alert level
- Class II
- Alert type
- recall
- Barcode (EAN/GTIN)
- 840682121446
- Brand on record
- GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING
What the authority reported
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.
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
US FDA — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.
Record last checked against the registry on 2026-05-31.
Other recalls from this brand
- 2025-12-24 · US FDA — Medical Devices
GE Healthcare Omni Legend, sold under the following names: OMNI Legend 16, Omni Legend 21, OMNI Legend 32, - 2025-12-10 · US FDA — Medical Devices
SMV DSI, System, Tomography, Computed, Emission - 2025-09-12 · US FDA — Medical Devices
Millenium MG/MC; dual-head nuclear medicine gamma camera designed specifically for cardiac imaging
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