ClearanceBrief
Recall Z-2727-2026 ยท IZL System, X-Ray, Mobile

GE Medical Systems, LLC

Optima XR220amx, Mobile Digital-Ready Radiographic System

DateJul 13, 2026 (initiated Jun 5, 2026)
StatusOpen, Classified
ReasonGE HealthCare has become aware that in certain Optima XR200/220/240amx systems that have had a column replacement completed, functional testing of the safety pawl may not have been performed to confirm proper assembly. If a failure of the internal counterpoise cable occurs, the Column Safety mechanism will not work, causing the arm with X-ray tube and collimator to drop downward on the column track. This could result in patient injury during an exam.
Root causeProcess control
ActionAn URGENT MEDICAL DEVICE CORRECTION notification letter dated 6/5/26 was sent to customers. Actions to be taken by Customer/User Pending corrections from GE HealthCare, you can continue to use the system by following the instructions below: Perform a check of your device prior to each patient exam to look for the following behaviors: "Column vertical movement requires increased effort. "Column has change in resistance (i.e. movement is not smooth) during vertical movement. "Column makes abnormal noises during vertical movement. If any are observed, DO NOT use the device and call GE HealthCare
Quantity38 units
DistributionWorldwide - US Nationwide and the countries of Brazil, Canada, Korea, Mexico, Saudi Arabia, Spain, UK.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K103476BRIVOXR285AMX, OPTIMA XR200AMX, OPTIMAXR220AMX
Ge Medical Systems, LLC, Jun 16, 2011
K142383Optima XR200amx, Optima XR220amx
Ge Medical Systems, LLC, Sep 25, 2014