Official recall record
GE Healthcare Innova IGS 5, computed tomography x-ray system
- Issuing authority
- US FDA — Medical Devices
- Alert date
- 2024-03-18
- Country of alert
- France
- Alert level
- Class II
- Alert type
- recall
- Barcode (EAN/GTIN)
- 00840682124621
- Brand on record
- GE Medical Systems, SCS
What the authority reported
GE HealthCare has become aware of the potential that adhesive material might not have been applied to some bolts of certain Innova IGS, Discovery IGS, Interact IGS, Allia IGS and Allia Pulse IGS products. This could result in a potential fall of the Detector/Elevator or X-ray tube of the frontal Gantry assembly.
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
- 2024-03-18 · US FDA — Medical Devices
GE Healthcare Allia IGS 7, Interventional fluoroscopic x-ray systems - 2024-03-18 · US FDA — Medical Devices
GE Healthcare Allia IGS 7 OR, Interventional fluoroscopic x-ray systems - 2024-03-18 · US FDA — Medical Devices
GE Healthcare Allia IGS 5 Pulse, Interventional fluoroscopic x-ray systems
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