# FDA recall Z-2733-2024

> **GE Healthcare (China) Co., Ltd.** · Class II · device recall initiated 2024-07-12.

## Product

GE Healthcare Proteus XR/a, stationary X-Ray System, Model/Catalog Numbers:    1) 2259973;   2) 2259988;   3) 2266999;   4) 2373519;   5) 2379827;   6) 5729352;   7) 2259973-1;   8) 2259973-2;   9) 2259973-3;   10) 2259973-4;   11) Not Available

## Reason for recall

The XR system, Proteus XR/a, does not have a de-installation manual describing process steps for de-installing the devices. De-installation instruction process steps must be followed when de-installing these devices to avoid personnel injury during de-install.

## Distribution

Worldwide distribution.

## Key facts

- **Recall number:** Z-2733-2024
- **Recalling firm:** GE Healthcare (China) Co., Ltd.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-07-12
- **Report date:** 2024-09-04

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Beijing, China

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2733-2024

## Citation

> AI Analytics. FDA recall Z-2733-2024. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-2733-2024. Source: US FDA. Licensed CC0.

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