GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING: Device Recall
Recall #Z-2098-2025 · 06/20/2025
Class II: Risk
Recall Details
- Recall Number
- Z-2098-2025
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING
- Status
- Ongoing
- Date Initiated
- 06/20/2025
- Location
- Tirat Carmel, N/A, Israel
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 21
Reason for Recall
Unintended radial detector motion may occur during patient setup or during patient scan if system does not have correct version of gantry software installed. Unintended detector motion may result in life-threatening injury.
Product Description
Varicam, Millennium VG, Millennium VG Hawkeye, Discovery VH Nuclear Medicine System
Distribution Pattern
Worldwide - US Nationwide distribution.
Other Recalls by GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING
- Class II: Risk 12/24/2025
- Class II: Risk 12/10/2025
- Class II: Risk 12/10/2025
- Class II: Risk 12/10/2025
- Class II: Risk 12/10/2025
View all recalls by GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING →
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.