# FDA recall Z-0703-2019

> **GE Healthcare, LLC** · Class II · device recall initiated 2017-10-30.

## Product

Discover VH/Millennium VG Nuclear Medicine Imaging System

## Reason for recall

A potential hazardous situation may occur if the collimator locking handle is not properly placed in the lock position and the warning circuit does not detect that the collimator is unlocked because of the patient proximity to the collimator during a clinical scan.

## Distribution

Worldwide

## Key facts

- **Recall number:** Z-0703-2019
- **Recalling firm:** GE Healthcare, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Completed
- **Initiation date:** 2017-10-30
- **Report date:** 2019-01-16

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Waukesha, WI, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0703-2019

## Citation

> AI Analytics. FDA recall Z-0703-2019. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-0703-2019. Source: US FDA. Licensed CC0.

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