GE Medical Systems, LLC

Frequent Recalls

16

Recalls

0

Units Recalled

0

Injuries

0

Deaths

Categories: Medical Device

2026-03-25 to 2026-06-17

Date	Source	Product	Brand	Severity	Units
2026-06-17	FDA Device	FDA Recall: Allia Moveo angiographic X-ray system	GE Medical Systems, LLC	Class II	N/A
2026-06-17	FDA Device	FDA Recall: Allia IGS 3 Pulse angiographic X-ray system	GE Medical Systems, LLC	Class II	N/A
2026-06-17	FDA Device	FDA Recall: Allia IGS 5 Pulse angiographic X-ray system	GE Medical Systems, LLC	Class II	N/A
2026-06-17	FDA Device	FDA Recall: Allia IGS 7 Pulse angiographic X-ray system	GE Medical Systems, LLC	Class II	N/A
2026-06-17	FDA Device	FDA Recall: Allia IGS Pulse angiographic X-ray system	GE Medical Systems, LLC	Class II	N/A
2026-05-20	FDA Device	FDA Recall: Revolution CT, x-ray computed tomography, Model Numbers 5590000 and 5590000-6	GE Medical Systems, LLC	Class II	N/A
2026-05-20	FDA Device	FDA Recall: Revolution Apex Elite, X-ray Computed Tomography, Model Number 5590000-23	GE Medical Systems, LLC	Class II	N/A
2026-05-20	FDA Device	FDA Recall: Revolution CT ES, X-ray Computed Tomography, Model Number 5590000-15	GE Medical Systems, LLC	Class II	N/A
2026-05-20	FDA Device	FDA Recall: Revolution Ascend, computed tomography, Model Numbers 6969000-100 and 6969000-300	GE Medical Systems, LLC	Class II	N/A
2026-05-20	FDA Device	FDA Recall: Revolution Apex Select, X-ray Computed Tomography, Model Number 5590000-27	GE Medical Systems, LLC	Class II	N/A
2026-05-20	FDA Device	FDA Recall: Revolution Apex, X-ray Computed Tomography, Model Number 5590000-20	GE Medical Systems, LLC	Class II	N/A
2026-05-20	FDA Device	FDA Recall: Revolution Apex Plus, X-ray Computed Tomography, Model Number 5590000-25	GE Medical Systems, LLC	Class II	N/A
2026-04-01	FDA Device	FDA Recall: Imactis CT-Navigation System, stereotaxic accessory for Computer Tomography (CT), systems, Model Num	GE Medical Systems, LLC	Class II	N/A
2026-03-25	FDA Device	FDA Recall: Centricity Universal Viewer Software Versions 7.0 through 7.0 Sp2.0.1, a device that displays medica	GE Medical Systems, LLC	Class II	N/A
2026-03-25	FDA Device	FDA Recall: Centricity Universal Viewer Software Versions 5.0 SP6 through UV 5.0 SP7.1, a device that displays m	GE Medical Systems, LLC	Class II	N/A
2026-03-25	FDA Device	FDA Recall: Centricity Universal Viewer Software Versions 6.0 through 6.0 Sp10.4.1, a device that displays medic	GE Medical Systems, LLC	Class II	N/A

GE Medical Systems, LLC Recalls | WatchRecall