# FDA recall Z-0856-2021

> **GE Healthcare, LLC** · Class II · device recall initiated 2020-12-10.

## Product

Discovery NM 630 (Model Number H3101RH), NM 830 (Model Number H3910AC), 830 NM Cyber Defense (Model Number H3910AG) - Product Usage: intended for general Nuclear Medicine imaging procedures for detection of radioisotope tracer uptake in the patient body.

## Reason for recall

GE Healthcare has become aware that rotor bearing screws were found loose on one detector in the field, leading to the release of one of the four rotor bearings in the detector.

## Distribution

Worldwide

## Key facts

- **Recall number:** Z-0856-2021
- **Recalling firm:** GE Healthcare, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2020-12-10
- **Report date:** 2021-01-20

- **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-0856-2021

## Citation

> AI Analytics. FDA recall Z-0856-2021. Retrieved 2026-07-02 from https://api.ai-analytics.org/recall/Z-0856-2021. Source: US FDA. Licensed CC0.

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