General Electric Med Systems LLC Patient tables of CT systems with brand name: CT/e; CT/e Dual; CT/e Plus, CT/e Dual Plus; CT/e Lite; ProSpeed AI; ProSpeed AII; ProSpeed FI; ProSpeed FII; ProSpeed EII; CT HiSpeed Series. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Patient tables of CT systems with brand name: CT/e; CT/e Dual; CT/e Plus, CT/e Dual Plus; CT/e Lite; ProSpeed AI; ProSpeed AII; ProSpeed FI; ProSpeed FII; ProSpeed EII; CT HiSpeed Series.
Brand
General Electric Med Systems LLC
Lot Codes / Batch Numbers
Model or Catalog: 2297024, 2320315, 2244226, 2113694-2, 2115992-4, 2200290-2
Products Sold
Model or Catalog: 2297024, 2320315, 2244226, 2113694-2, 2115992-4, 2200290-2
General Electric Med Systems LLC is recalling Patient tables of CT systems with brand name: CT/e; CT/e Dual; CT/e Plus, CT/e Dual Plus; CT/e Lite; due to The patient tables of the affected CT systems are supported by a hydraulic cylinder and a cylinder shaft (i.e. the upper shaft) which connects the tab. Based on FDA medical device recall database.
Summary derived from FDA notice
The following details were not provided by the FDA: distribution information.
Reason for Recall
As stated by FDA
The patient tables of the affected CT systems are supported by a hydraulic cylinder and a cylinder shaft (i.e. the upper shaft) which connects the tabletop to the table frame. GE received a report of a HiSpeed LX/I system table falling abruptly due to the filure of the upper shaft. No injuries were reported.
Recommended Action
Per FDA guidance
Inadequate materials used to manufacture the upper shaft of patient tables that can result in uncontrolled table motion.
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