Medical DevicesNationwide
GE OEC Medical Systems, Inc RUS Tool Version Software Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
RUS Tool Version Software
Brand
GE OEC Medical Systems, Inc
Lot Codes / Batch Numbers
All versions prior to Version 7.1.43.
Products Sold
All versions prior to Version 7.1.43.
GE OEC Medical Systems, Inc is recalling RUS Tool Version Software due to X-ray systems could provide output which exceeds the 20 R/minute limit.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
X-ray systems could provide output which exceeds the 20 R/minute limit.
Recommended Action
Per FDA guidance
Consignees were notified by certified letter on 08/14-15/2006.
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 noticePage updated: Jan 10, 2026