Z-2386-2018 Class II Terminated

Recalled by GE Medical Systems, SCS — Buc

Recall Details

Product Type
Devices
Report Date
July 18, 2018
Initiation Date
March 29, 2018
Termination Date
June 15, 2021
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
102 devices total

Product Description

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 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.

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).