Ge Inspection Technologies Llc v|tome|x L Series non-destructive testing cabinet x-ray systems Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
v|tome|x L Series non-destructive testing cabinet x-ray systems
Brand
Ge Inspection Technologies Llc
Lot Codes / Batch Numbers
v/tome/x L Series (L240, L300 or L450)
Products Sold
v/tome/x L Series (L240, L300 or L450)
Ge Inspection Technologies Llc is recalling v|tome|x L Series non-destructive testing cabinet x-ray systems due to It was discovered during testing of the v/tome/x L450 system s/n PA1790, that the pre-warning signals does not provide "Audible and visible warning s. Based on FDA medical device recall database.
Summary derived from FDA notice
The following details were not provided by the FDA: corrective action details.
Reason for Recall
As stated by FDA
It was discovered during testing of the v/tome/x L450 system s/n PA1790, that the pre-warning signals does not provide "Audible and visible warning signals within the cabinet" if the "warm up" mode was not completed after initializing the system when first turned on.
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 noticePage updated: Jan 10, 2026