Varicam, Millennium VG, Millennium VG Hawkeye, Discovery VH Nuclear Medicine System
FDA device recall Z-2098-2025 · posted 2025-07-08 · Open, Classified
Recall details
- Recalling firm
- GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING
- 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.
- Action taken
- Firm notified customers via Urgent Medical Device Correction letter dated June 20, 2025. Customers were instructed to check gantry software version. Instructions to do so are included in the letter. If system has the correct gantry software version, customers may continue to use their system--V.25BK for Infinia Running on Windows2000 (Win2K); C.15BK or C.1523 for Infinia on Windows XP; V.60BK on VG (all operating systems). If the software version is not the correct version, customers should discontinue use of system and contact GE HealthCare Service or local Service Representative. GE HealthCare will correct systems at no cost to the customer. Correction will include a hardware update and, if necessary, a software update. GE HealthCare representatives will contact customers to arrange for the correction. If you have any questions or concerns regarding this notification, please contact GE HealthCare Service at 1-800-437-1171 or your local Service Representative.
- Root cause
- Software design
- Status
- Open, Classified
- Product code
- KPS
- Quantity affected
- 21
- Distribution
- Worldwide - US Nationwide distribution.
- Date initiated
- 2025-06-20
- Date posted
- 2025-07-08
- Location
- Tirat Carmel, Israel
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Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| VARICAM (K953801) | Elscint, Inc. | 1995-11-22 |