GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING: Device Recall

Recall #Z-1044-2026 · 12/10/2025

Class II: Risk

Recall Details

Recall Number
Z-1044-2026
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
7 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 DSX New Line, System, Tomography, Computed, Emission

Distribution Pattern

US, Brazil, Egypt, Canada, Mexico, Turkey, Italy, Sweden, Switzerland, France, Spain Chile, Germany, Iran, Greece

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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.