Discovery IGS 740 Interventional Fluoroscopic X-ray Systems — Class II medical device recall Z-2388-2018
Terminated recall by GE Medical Systems, SCS, reported 2018-07-18, distributed in AR, CA, FL, GA, IA, IL, NC, NH…. The Discovery IGS and Innova IGS systems may experience X-ray abort errors which could result in the loss of i
| Recall number | Z-2388-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | GE Medical Systems, SCS, Buc, France |
| Recall initiated | 2018-03-29 |
| Classified | 2018-07-06 |
| Reported by FDA | 2018-07-18 |
| Terminated | 2021-06-15 |
| Distributed | AR, CA, FL, GA, IA, IL, NC, NH, NJ, NM, NY, PA, SC, TN, WI, WV |
| Countries outside the US | AR, BR, CN, CO, EG, ES, FR, GB, ID, IN, IR, IT, JP, KW, LT, PL, RU, SA, SG, TN, TR, VN |
| Quantity | 102 devices |
| Lot numbers | 00000D4-17-029, 00000D4-17-030, 00000D4-17-031, 00000D4-17-032, 00000D4-18-001, 00000D4-18-003 |
| Model numbers | 00000D4-17-028, 5730891, 5759342 |
Product
Discovery IGS 740 Interventional Fluoroscopic X-ray Systems
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2388-2018. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.