FDA Device recall Z-2386-2018
Discovery IGS 730 Interventional Fluoroscopic X-ray Systems
- FDA Device
- Class II
- terminated
- Published 2018-07-18
On 2018-07-18 the FDA classified a Class II recall of Discovery IGS 730 Interventional Fluoroscopic X-ray Systems by Ge Medical Systems Scs, citing the Discovery IGS and Innova IGS systems may experience X-ray abort errors which could result in the loss of imaging mode before or during fluoroscopic use.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2386-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-03-29 |
| Published | 2018-07-18 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Ge Medical Systems Scs |
| Distribution | AR, CA, FL, GA, IA, IL, NC, NH, NJ, NM, NY, PA, SC, TN, WI, WV |
Product
Discovery IGS 730 Interventional Fluoroscopic X-ray Systems
Reason
The Discovery IGS and Innova IGS systems may experience X-ray abort errors which could result in the loss of imaging mode before or during fluoroscopic use.
Identifiers
| code_info | Model Number 5730890, Serial Numbers (System ID): 00000D3-17-030 (904BHHCHY), 00000D3-17-032 (083172440628), 661327IGS…Model Number 5730890, Serial Numbers (System ID): 00000D3-17-030 (904BHHCHY), 00000D3-17-032 (083172440628), 661327IGS730 (00000D3-18-001), GON4598369 (00000D3-18-004), 082416140028 (00000D3-17-025), M4234253 (00000D3-17-028), YV3601 (00000D3-18-005), 6073XR0058 (00000D3-17-031). |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2386-2018%22
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