GE Healthcare Proteus XR/a — Class II medical device recall Z-2733-2024
Ongoing recall by GE Healthcare (China) Co., Ltd., reported 2024-09-04. The XR system, Proteus XR/a, does not have a de-installation manual describing process steps for de-installing
| Recall number | Z-2733-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | GE Healthcare (China) Co., Ltd., Beijing, China |
| Recall initiated | 2024-07-12 |
| Classified | 2024-08-26 |
| Reported by FDA | 2024-09-04 |
| Quantity | 3,572 units |
| UPC / GTIN / UDI-DI | 00840682106139, 00840682120777 |
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2733-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.