GE Inspection Technologies, LP GE Cabinet X-ray systems Recall
Class II: A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Class II recall indicates potential for temporary health effects.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
GE Cabinet X-ray systems
Brand
GE Inspection Technologies, LP
Lot Codes / Batch Numbers
XXL cabinet x-ray systems, serial numbers A586590 and A586780, xlcube compact cabinet x-ray systems, serial numbers A583730, A586430, and A586460, a VTOMEX C450 cabinet x-ray system, serial number VTXO1JOOO2-2245 14, VTOMEX L300 cabinet x-ray systems, serial numbers VTX01lF007-208813, VTX01F007-196312 and VTXO1FOO07-1946 12, and VTOMEX L450 cabinet x-ray systems, serial numbers VTXO1K0001-184711 and PX_10E000-179013.
Products Sold
XXL cabinet x-ray systems, serial numbers A586590 and A586780; xlcube compact cabinet x-ray systems, serial numbers A583730, A586430, and A586460; a VTOMEX C450 cabinet x-ray system, serial number VTXO1JOOO2-2245 14; VTOMEX L300 cabinet x-ray systems, serial numbers VTX01lF007-208813, VTX01F007-196312 and VTXO1FOO07-1946 12; and VTOMEX L450 cabinet x-ray systems, serial numbers VTXO1K0001-184711 and PX_10E000-179013.
GE Inspection Technologies, LP is recalling GE Cabinet X-ray systems due to GE discovered these cabinet x-ray systems' potential failure to comply with the Cabinet X-ray System performance standards.. This is a Class I recall, indicating a high risk of serious health consequences or death. Based on FDA medical device enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
GE discovered these cabinet x-ray systems' potential failure to comply with the Cabinet X-ray System performance standards.
Recommended Action
Per FDA guidance
Healthcare providers and patients should stop using the device and contact the manufacturer for further instructions. Report problems to FDA MedWatch.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
CA, IN, MI, NH, NC, OR, PA, SC, WA
Page updated: Jan 13, 2026