GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING: Device Recall

Recall #Z-0891-2025 · 12/18/2024

Class II: Risk

Recall Details

Recall Number
Z-0891-2025
Classification
Class II
Product Type
Device
Recalling Firm
GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING
Status
Ongoing
Date Initiated
12/18/2024
Location
Tirat Carmel, Israel
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
859 units

Reason for Recall

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.

Product Description

GE 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, Computed, Emission

Distribution Pattern

Worldwide

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Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.