# FDA recall Z-0379-2018

> **Carl Zeiss Metrology Inc** · Class II · device recall initiated 2017-11-14.

## Product

Metrotom 800 (130kV CT scanner)    Industrial CT scanner for measuring and inspecting complete components made of plastic or light metal.

## Reason for recall

Due to a software error, it was observed that when the user closes the access door, the system will resume its scan cycle automatically, instead of the user initiating x-ray generation from the control panel.

## Distribution

Worldwide Distribution - US, including the states of :  WI, NC, GA, IL, AZ, FL, CA, NJ, and territory of PR; and the country of Canada.

## Key facts

- **Recall number:** Z-0379-2018
- **Recalling firm:** Carl Zeiss Metrology Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2017-11-14
- **Report date:** 2018-02-07

- **Voluntary/Mandated:** FDA Mandated
- **Location:** Maple Grove, MN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0379-2018

## Citation

> AI Analytics. FDA recall Z-0379-2018. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-0379-2018. Source: US FDA. Licensed CC0.

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