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Terminated

v|tome|x L Series non-destructive testing cabinet x-ray systems

FDA Recall Z-0442-2021 · Posted None

Recalling FirmGe Inspection Technologies Llc
Recall StatusTerminated
Product CodeRCE
Date Initiated2020-09-29
Date Terminated2023-05-02

Reason for Recall

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.

Root Cause

Radiation Control for Health and Safety Act

Distribution Pattern

USA Canada

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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