GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING: Device Recall
Recall #Z-1046-2026 · 12/10/2025
Recall Details
- Recall Number
- Z-1046-2026
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING
- Status
- Ongoing
- Date Initiated
- 12/10/2025
- Location
- Tirat Carmel, Israel
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 12 units
Reason for Recall
GE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service (herein referred to as Impacted Systems and listed in the Affected Product Details section of this letter) could have been transported or relocated without adequate detector support. This could result in excessive stress being applied to the detector mounting mechanisms, compromising their integrity. If this occurs, it can potentially result in a detector fall and lead to life-threatening bodily injury. There have been no reports of detector falls or injuries as a result of this potential issue. The Impacted Systems affected by this notice are those that have not been manufactured for several years. GE HealthCare has previously communicated End of Guaranteed Service for these Impacted Systems.
Product Description
SMV BodyTrack, System, Tomography, Computed, Emission
Distribution Pattern
US, Brazil, Egypt, Canada, Mexico, Turkey, Italy, Sweden, Switzerland, France, Spain Chile, Germany, Iran, Greece
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 09/12/2025
View all recalls by GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING →