Ge Healthcare GE Healthcare Fluorostar 7900 Mobile Fluoroscopy System Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
GE Healthcare Fluorostar 7900 Mobile Fluoroscopy System
Brand
Ge Healthcare
Lot Codes / Batch Numbers
n/a
Products Sold
n/a
Ge Healthcare is recalling GE Healthcare Fluorostar 7900 Mobile Fluoroscopy System due to The alarm timer is reset after each exposure and therefore never reaches the five minute alarm state unless one exposure exceeds 5 minutes in duration. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The alarm timer is reset after each exposure and therefore never reaches the five minute alarm state unless one exposure exceeds 5 minutes in duration.
Recommended Action
Per FDA guidance
GE Healthcare sent a customer notification out to all sites that have potentially affected systems. GEHC Surgery will also install a software correction into the affected systems in order to resolve this issue at no charge to the customer. Until the GEHC OEC Fluorostar 7900 has received the corrective software installed, they are encouraging facilities to exercise caution in monitoring the amount of cumulative fluoroscopy time when the affected system is in use.
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