- Recalling firm
- GE Medical Systems, LLC
- Reason for recall
- GE 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.
- Affected products (lot / model / serial)
- UDI-DI: 00840682115278; System IDs: 419383DP3, 773792XR200, 856355OPT, FEB520100
- Units affected
- 4 units
- Distribution pattern
- Worldwide - US Nationwide and the countries of Brazil, Canada, Korea, Mexico, Saudi Arabia, Spain, UK.
- Firm location
- Waukesha, WI, United States
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- Letter
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-2726-2026
- Recall initiated
- June 5, 2026
- FDA classification date
- July 13, 2026
- FDA report date
- July 22, 2026
- FDA event ID
- 99279
- Last updated on HTM Vibe
- July 28, 2026