# FDA recall Z-1748-2019

> **GE Healthcare, LLC** · Class II · device recall initiated 2019-02-12.

## Product

Discovery IQ     Product Usage: The systems are intended for head and whole body attenuation corrected Positron Emission  Tomography (PET) imaging and localization of emission activity in patient anatomy by means of  integrated PET and CT images.

## Reason for recall

GE Healthcare PET/CT Table Stop Without Stopping X-Ray Exposure

## Distribution

Nationwide Distribution

## Key facts

- **Recall number:** Z-1748-2019
- **Recalling firm:** GE Healthcare, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2019-02-12
- **Report date:** 2019-06-26

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1748-2019

## Citation

> AI Analytics. FDA recall Z-1748-2019. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-1748-2019. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*