FDA Device recall Z-1779-2024
GE Healthcare Interact Discovery RT, Interventional fluoroscopic x-ray systems
- FDA Device
- Class II
- ongoing
- Published 2024-05-15
On 2024-05-15 the FDA classified a Class II recall of GE Healthcare Interact Discovery RT, Interventional fluoroscopic x-ray systems by Ge Medical Systems Scs, citing 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….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1779-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-03-18 |
| Published | 2024-05-15 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Ge Medical Systems Scs |
| Distribution | US |
Product
GE Healthcare Interact Discovery RT, Interventional fluoroscopic x-ray systems
Reason
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.
Identifiers
| code_info | UDI/DI 00840682141581, Serial Numbers: M4-23-049 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1779-2024%22
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