# FDA recall Z-2777-2017

> **GE Inspection Technologies, LP** · Class II · device recall initiated 2017-06-28.

## Product

GE Inspection Technologies Blade|line Industrial Cabinet X-ray system

## Reason for recall

GE Inspection Technologies, LP determined that the Blade|line cabinet x-ray system fails to comply with the cabinet x-ray performance standards emission limit of 0.5 milliRoentgen in one hour (21 CFR ¿ 1020.40(c)(1)(i)) underneath the bottom center of the system.  The crawl space affected by the excess emission is approximately 22 inches high, normally covered by decorative panels, and is not intended to be accessed.

## Distribution

US Distribution to the states of : AL, SC, OH, MI, PA, and Internationally to Germany and Singapore

## Key facts

- **Recall number:** Z-2777-2017
- **Recalling firm:** GE Inspection Technologies, LP
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-06-28
- **Report date:** 2017-08-09
- **Termination date:** 2020-02-06

- **Voluntary/Mandated:** FDA Mandated
- **Location:** Lewistown, PA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2777-2017

## Citation

> AI Analytics. FDA recall Z-2777-2017. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-2777-2017. Source: US FDA. Licensed CC0.

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