# FDA recall Z-1783-2024

> **GE Medical Systems, SCS** · Class II · device recall initiated 2024-03-18.

## Product

GE Healthcare Allia IGS 5 Pulse,  Interventional fluoroscopic x-ray systems

## Reason for recall

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.

## Distribution

Worldwide distribution - US Nationwide in the states of CA, FL, GA, IN, MA, NC, OK, SC, TN, TX, VA and the countries of Armenia, China, France, Hungary, India, Italy, Japan, Kazakhstan, Lithuania, Mexico, Russia, Spain, Taiwan, Turkey, Vietnam

## Key facts

- **Recall number:** Z-1783-2024
- **Recalling firm:** GE Medical Systems, SCS
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-03-18
- **Report date:** 2024-05-15

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1783-2024

## Citation

> AI Analytics. FDA recall Z-1783-2024. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-1783-2024. Source: US FDA. Licensed CC0.

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