ClearanceBrief
Recall Z-0813-2025 ยท IZL System, X-Ray, Mobile

GE Medical Systems, LLC

GE Healthcare Optima XR240amx, Mobile Digital Radiographic System, Model Numbers: 1) 5555000-27; 2) 5555000-31; 3) 5555000-33; 4) 5555000-41; 5) 5555000-47; 6) A0700DL; 7) A1700DA; 8) To be provided.

DateJan 7, 2025 (initiated Nov 25, 2024)
StatusOpen, Classified
ReasonGE HealthCare has become aware that in certain Optima XR200/220/240amx systems that have had a column replacement performed, some bolts used in the Column Safety mechanism can be missing. If these bolts are missing and a failure of the internal counterpoise cable occurs, the Column Safety mechanism will not work properly causing the arm with X-ray tube and collimator to drop downward on the column track.
Root causeComponent design/selection
ActionGE Healthcare issued an URGENT MEDICAL DEVICE CORRECTION notice to its consignees on 11/25/2024 via letter issued using traceable means. The notice explained the issue, safety issue, and requested the following actions be taken by the user: "1. Perform a check of your device prior to each patient exam to look for the following behaviors. If any are observed, DO NOT use the device and call GE HealthCare Service Immediately. . Column vertical movement requires increased effort. . Column has change in resistance (i.e. movement is not smooth) during vertical movement. . Column makes abnormal no
Quantity120 units
DistributionWorldwide
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K162990Optima XR240amx
Ge Medical Systems, LLC, Nov 15, 2016
K173602Optima XR240amx, AutoGrid
Ge Medical Systems, LLC, Jan 12, 2018
K182234Optima XR240amx
Ge Medical Systems, LLC, Sep 6, 2018