GE Medical Systems, SCS: Medical Device Recall in 2018 - (Recall #: Z-2388-2018)

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 740 Interventional Fluoroscopic X-ray Systems

Product Classification:

Class II

Date Initiated: March 29, 2018

Date Posted: July 18, 2018

Recall Number: Z-2388-2018

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 5730891- Lot Number (System ID): 00000D4-17-029 (478765NSP), 00000D4-17-031 (712279DIS), 00000D4-17-030 (716845DISC), 00000D4-18-003 (951TVHDISC740), 00000D4-18-001 (352751DISC), 00000D4-17-032 (SA1011VA02); Model Number 5759342 - 00000D4-17-028 (GON 4610398).

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