Official recall record
GE Healthcare Proteus XR/a, stationary X-Ray System, Model/Catalog Numbers: 1) 2259973; 2) 2259988; 3) 2266999; 4) 2373519; 5) 23
- Issuing authority
- US FDA — Medical Devices
- Alert date
- 2024-07-12
- Country of alert
- China
- Alert level
- Class II
- Alert type
- recall
- Barcode (EAN/GTIN)
- 00840682120777
- Brand on record
- GE Healthcare (China) Co., Ltd.
What the authority reported
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.
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
US FDA — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.
Record last checked against the registry on 2026-05-31.
Same barcode in other registries
The same EAN appears in 1 other official recall record(s) — a cross-border signal worth checking if you bought this product abroad.
- 2024-10-24 · US FDA — Medical Devices
GE Proteus XR/A radiographic system
Other recalls from this brand
- 2025-01-31 · US FDA — Medical Devices
SIGNA MR355, SIGNA MR360, NMRI system - 2025-01-31 · US FDA — Medical Devices
SIGNA Creator, SIGNA Explorer, NMRI systems - 2025-01-31 · US FDA — Medical Devices
Brivo MR355, NMRI system
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