Ge Inspection Technologies recalls L Series non-destructive testing x-ray systems that may not emit audible or visible warnings if warm-up mode isn't completed after initial startup.
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.
Ge Inspection Technologies is recalling v|tome|x L Series non-destructive testing x-ray systems because they may not provide audible or visible warnings if the warm-up mode isn't completed after first turning on. This could lead to users not being alerted to potential issues during operation.
The systems may not emit audible or visible warnings if the warm-up mode isn't completed after initial startup. This means users might not be alerted to potential issues during operation, which could lead to unsafe conditions.
Users of v|tome|x L Series non-destructive testing cabinet x-ray systems (L240, L300, L400 models) are affected. Those operating these systems in industrial or safety inspection settings are most at risk.
Check for v|tome|x L Series non-destructive testing cabinet x-ray systems with model numbers L240, L300, or L400. These were sold by Ge Inspection Technologies.
Ensure the system completes warm-up mode after initial startup to activate warning signals.
The recall does not require immediate stop use; users can continue operating with proper warm-up checks.
L240, L300, and L400 models of v|tome|x L Series non-destructive testing cabinet x-ray systems.
The recall record does not specify a fix or remedy.
We’ve drafted a message you can send Ge Inspection Technologies to request your refund or repair — edit it as you like.
Subject: Recall Z-0442-2021 — Ge Inspection Technologies Ge Inspection Technologies Hello, I own a Ge Inspection Technologies that is covered by recall Z-0442-2021 from Ge Inspection Technologies. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
