# FDA recall Z-2386-2018

> **GE Medical Systems, SCS** · Class II · device recall initiated 2018-03-29.

## Product

Discovery IGS 730 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.

## Distribution

US distribution: AR, CA, CA, FL, GA, IA, IL, NC, NH, NJ, NM, NY, PA, SC, TN, A,WI, WV.      International Distribution: Argentina, Brazil, China, Colombia, Egypt, France, India, Indonesia, Iran, Italy, Japan, Kuwait, Lithuania, Myanmar, Palestine, Poland, Russia, Saudi Arabia, Singapore, Spain, Tunisia, Turkey, United Kingdom, Vietnam.

## Key facts

- **Recall number:** Z-2386-2018
- **Recalling firm:** GE Medical Systems, SCS
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-03-29
- **Report date:** 2018-07-18
- **Termination date:** 2021-06-15

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Buc, France

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2386-2018

## Citation

> AI Analytics. FDA recall Z-2386-2018. Retrieved 2026-05-29 from https://api.ai-analytics.org/recall/Z-2386-2018. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*