Recall Register

GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING: FDA recalls

FDA enforcement reports name GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING as the recalling firm in 7 events. The events have 41 product records. The recalls started from 2022 to 2025. All the events are device recalls.

It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.

FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .

Enforcement events

7 events, newest first.

FDA enforcement events of GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING
InitiatedProduct (first record)TypeClassRecordsStatus
24 Dec 2025GE Healthcare Omni Legend, sold under the following names: OMNI Legend 16, Omni Legend 21, OMNI Legend 32, Omni Legend PET Gantry 16cm - MEA, Omni Legend PET Gantry 16cm Haifa LM, Omni Legend PET Gantry 16cm Mobile, Omni Legend PET Gantry 21cm - BJ for Global, Omni Legend PET Gantry 21cm - Global Haifa LM, Omni…DeviceClass II1Completed
10 Dec 2025SMV DSX New Line, System, Tomography, Computed, EmissionDeviceClass II4Ongoing
12 Sep 2025Elscint Cardial; dual-head nuclear medicine gamma camera designed specifically for cardiac imagingDeviceClass II14Ongoing
20 Jun 2025Infinia, Infinia Hawkeye, Infinia II, Infinia II Hawkeye 4 Nuclear Medicine systemDeviceClass II2Ongoing
18 Dec 2024GE Healthcare Infinia I, Model/Catalog Numbers: 1) 5178728, 2) H3000WE, 3) H3000WM, 4) H3000YG; System, Tomography, Computed, EmissionDeviceClass II13Ongoing
15 Apr 2024MyoSPECT System, Model H3912AA and H3912B, and MyoSPECT ES System, Model H3912AB and H3912BD, dedicated cardiac SPECT (single photon emission computerized tomography system).DeviceClass II1Ongoing
19 Dec 2022GE Nuclear Medicine 600/800 series systems, specifically: a) 870, b) 870 DR 3/8 inch NM GANTRY WITH NEW ROTOR - MEA, c) 870 DR / Dismount, d) 870 DR / Dismount / 60HZ, e) 870 DR 3/8 inch WSO, f) 870 DR 3/8 inch NM Gantry, g) 870 DR 3/8 inch, h) 870 DR 3/8 inch CH, i) 870 DR 5/8 inch NM GANTRY, j) 870 DR BJ /…DeviceClass I6Ongoing

An event with 1 product record and a class that is not Class I has no page. It has a row in this table.

Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.

Recalling firm: The firm that the FDA record names for a recall.

Type and class

GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING: events for each product type
TypeEvents
Device7
GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING: events in each class
ClassEvents
Class II6
Class I1
Share of the events of the firm in Class I
14%
Share of all events on the register in Class I
18%
Events with the status Ongoing
6

openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports. Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.

Events by year

FDA enforcement events of GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING, by the year that the recall started. The largest year is 2025, with 4 events.

Official channels

Cite this page

Recall Register. GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING: FDA recalls. https://recallregister.com/firm/ge-medical-systems-israel-functional-imaging/. Source: openFDA enforcement reports. Data through .

Sources

Source
openFDA enforcement reports
Licence
CC0 1.0
Export date
28 Sep 2026
State of the firm address
N/A

The firm name is the spelling in the FDA records. A company with 2 spellings has 2 pages.

A firm with more products can have more recalls. This site does not compare one firm with a different firm. How the register is made. Report an error.

Questions

Which classes do the FDA recalls of GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING have?
Class II: 6 events. Class I: 1 event. The class is for the product of a recall. It is not a class of the firm.
What is the newest FDA recall of GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING?
FDA event 98269, which the firm started on 24 Dec 2025. The first product in the record is: GE Healthcare Omni Legend, sold under the following names: OMNI Legend 16, Omni Legend 21, OMNI Legend 32, Omni Legend PET Gantry 16cm - MEA, Omni Legend PET Gantry 16cm Haifa LM, Omni Legend PET Gantry 16cm Mobile, Omni Legend PET Gantry 21cm - BJ for Global, Omni Legend PET Gantry 21cm - Global Haifa LM, Omni…
How many FDA recalls of GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING have the status Ongoing?
6 events have the status Ongoing in the openFDA file. openFDA says about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports.