GE Medical Systems, SCS: Medical Device Recall in 2018 - (Recall #: Z-2386-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

Discovery IGS 730 Interventional Fluoroscopic X-ray Systems

Product Classification:

Class II

Date Initiated: March 29, 2018

Date Posted: July 18, 2018

Recall Number: Z-2386-2018

Event ID: 80177

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.

Status: Terminated

Product Quantity: 102 devices total

Code Information:

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).

Distribution Pattern:

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.

Voluntary or Mandated:

Voluntary: Firm initiated