GE OEC Medical Systems, Inc GE OEC 8800 Fluoroscopic X-ray System, GE Healthcare, Salt Lake City, Utah Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
GE OEC 8800 Fluoroscopic X-ray System, GE Healthcare, Salt Lake City, Utah
Brand
GE OEC Medical Systems, Inc
Lot Codes / Batch Numbers
Serial Numbers: 7315PU5, 7372PU6, 7384PU1, 7385PU8, 7389PU0, 7390PU8, 7393PU2, 7398PU1, 7398PU1, 7399PU9, 7702PU4, 7720PU6, 7721PU4, 7724PU8, 7725PU5, 7726PU3, 7728PU9, 7729PU7, 7732PU1, 7733PU9, 7734PU7.7747PU9.
Products Sold
Serial Numbers: 7315PU5, 7372PU6, 7384PU1, 7385PU8, 7389PU0, 7390PU8, 7393PU2, 7398PU1, 7398PU1, 7399PU9, 7702PU4, 7720PU6, 7721PU4, 7724PU8, 7725PU5, 7726PU3, 7728PU9, 7729PU7, 7732PU1, 7733PU9, 7734PU7.7747PU9.
GE OEC Medical Systems, Inc is recalling GE OEC 8800 Fluoroscopic X-ray System, GE Healthcare, Salt Lake City, Utah due to X-ray systems were not configured to display Air Kerma Rate and Cumulative Air Kerma.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
X-ray systems were not configured to display Air Kerma Rate and Cumulative Air Kerma.
Recommended Action
Per FDA guidance
Consignees were notified by letter on 06/12/2007 and told that a service representative would arrange for an inspection and would modify their systems.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
CO, FL, GA, MD, PA, VA, WA
Page updated: Jan 10, 2026