General Electric Med Systems Performix X-ray Tube - Performix ADV, Performix Ultra, Solarix 630. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Performix X-ray Tube - Performix ADV, Performix Ultra, Solarix 630.
Brand
General Electric Med Systems
Lot Codes / Batch Numbers
Tube Catalog #''s D3132, D3172, D3182, and D3152 used on Gantry model #''s 2137130, 2137130-5, 2234921-3, 2260619, 2260619-3, 2281177, 2281177-2, 2281177-3, 2281177-4, 2305500, 2339985, 2341799, 2362605, and 5101272.
Products Sold
Tube Catalog #''s D3132, D3172, D3182, and D3152 used on Gantry model #''s 2137130, 2137130-5, 2234921-3, 2260619, 2260619-3, 2281177, 2281177-2, 2281177-3, 2281177-4, 2305500, 2339985, 2341799, 2362605, and 5101272.
General Electric Med Systems is recalling Performix X-ray Tube - Performix ADV, Performix Ultra, Solarix 630. due to Incorrect mounting hardware may cause X-ray tube to separate from the gantry and fall.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Incorrect mounting hardware may cause X-ray tube to separate from the gantry and fall.
Recommended Action
Per FDA guidance
Field Modification Instructions (FMI''s) will be issued to the field to inspect and locate suspect tubes and replace any that may be susceptible to failure.
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