GE Medical Systems LLC Definium AMX 700 Digital mobile x-ray system, GE Healthcare 3000 North Grandview Waukesha, WI Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Definium AMX 700 Digital mobile x-ray system, GE Healthcare 3000 North Grandview Waukesha, WI
Brand
GE Medical Systems LLC
Lot Codes / Batch Numbers
973971AMXD1, 973971AMXD2, 402449CDP1, 402449CDP2, 601426DAMX1, and 972566D700A
Products Sold
973971AMXD1, 973971AMXD2, 402449CDP1, 402449CDP2, 601426DAMX1, and 972566D700A
GE Medical Systems LLC is recalling Definium AMX 700 Digital mobile x-ray system, GE Healthcare 3000 North Grandview Waukesha, WI due to When using the Tech Switch on exposures >750ms, >100 kVp and > 100 mAs the exposure terminates prematurely.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
When using the Tech Switch on exposures >750ms, >100 kVp and > 100 mAs the exposure terminates prematurely.
Recommended Action
Per FDA guidance
Visit to each consignee beginning December 21, 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 noticeDistribution
As reported by FDA
IN, MS, NE, NJ, TX
Page updated: Jan 10, 2026