Official recall record
Discovery XR656 HD. X-Ray imaging system.
- Issuing authority
- US FDA — Medical Devices
- Recall initiated by firm
- 2025-01-28
- Country of alert
- United States
- Alert level
- Class II
- Alert type
- recall
- Barcode (EAN/GTIN)
- 00195278118356
- Brand on record
- GE Medical Systems, LLC
What the authority reported
The user can continue to take the next exposure after reaching the Automatic Exposure Control (AEC) limit, without taking any further actions to acknowledge or adjust exposure techniques. In all cases, a message still appears on the screen when the AEC limit is reached.
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.
Other recalls from this brand
- 2026-06-05 · US FDA — Medical Devices
Optima XR200amx, Mobile Digital-Ready Radiographic System - 2026-06-05 · US FDA — Medical Devices
Optima XR240amx, Mobile Digital Radiographic System - 2026-06-05 · US FDA — Medical Devices
Optima XR220amx, Mobile Digital-Ready Radiographic System
All 62 official recall notices naming GE Medical Systems, LLC on this site →
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