# FDA recall Z-0442-2021

> **Ge Inspection Technologies Llc** · Class II · device recall initiated 2020-09-29.

## Product

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

## 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.

## Distribution

USA  Canada

## Key facts

- **Recall number:** Z-0442-2021
- **Recalling firm:** Ge Inspection Technologies Llc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-09-29
- **Report date:** 2020-11-25
- **Termination date:** 2023-05-02

- **Voluntary/Mandated:** FDA Mandated
- **Location:** Skaneateles Falls, NY, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0442-2021

## Citation

> AI Analytics. FDA recall Z-0442-2021. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-0442-2021. Source: US FDA. Licensed CC0.

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