ProductGuru Recalls

Official recall record

Definium 656HD & Discovery XR656HD (GTINs: 00840682138598, 00195278840226, 00840682136709). X-Ray imaging system.

US FDA — Medical Devices · 2025-01-28 · United StatesClass II
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)
00840682138598
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.

More recalls: US FDA — Medical Devices · United States · all filters

Other recalls from this brand

All 62 official recall notices naming GE Medical Systems, LLC on this site →

ProductGuru Recalls republishes official safety information with attribution. We are not the issuing authority and this page is not advice. If this product is a medical device or medication, speak to a doctor or pharmacist. Found an error? Report it — corrections are published.