Fischer Imaging Corporation VersaRad Generator Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
VersaRad Generator
Brand
Fischer Imaging Corporation
Lot Codes / Batch Numbers
Generator S/N''s: 9918-0704-002, 9918-0804-003, 9918-0804-007, 9918-0804-005, 9918-0204-001, 9918-0304-001, 9918-0304-003, 9918-03304-004, 9918-0505-002, 9918-0604-001, 9918-0604-003, 9918-0604-006, 9918-0704-001, 9918-0704-003, 9918-0704-004, 9918-0704-005, 9918-0803-002, 9918-0804-002, 9918-0903-002, 9918-1003-001, 9918-1203-002, 9918-0604-007, 9918-0804-004, 9918-0404-002, 9918-0803-001, 9918-0504-003, 0304-002, 0404-003, 0504-004, 9918-0604-005, 9918-0903-001, 9918-0404-001, 9918-0604-002, 9918-0504-001, 9918-0804-001, 9918-1103-001, 9918-1203-001, 9918-0604-004.
Products Sold
Generator S/N''s: 9918-0704-002; 9918-0804-003; 9918-0804-007; 9918-0804-005; 9918-0204-001; 9918-0304-001; 9918-0304-003; 9918-03304-004; 9918-0505-002; 9918-0604-001; 9918-0604-003; 9918-0604-006; 9918-0704-001; 9918-0704-003; 9918-0704-004; 9918-0704-005; 9918-0803-002; 9918-0804-002; 9918-0903-002; 9918-1003-001; 9918-1203-002; 9918-0604-007; 9918-0804-004; 9918-0404-002; 9918-0803-001; 9918-0504-003; 0304-002; 0404-003; 0504-004; 9918-0604-005; 9918-0903-001; 9918-0404-001; 9918-0604-002; 9918-0504-001; 9918-0804-001; 9918-1103-001; 9918-1203-001; 9918-0604-004.
Fischer Imaging Corporation is recalling VersaRad Generator due to Some VersaRad Systems have a faulty weld that may result in oil leakage.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Some VersaRad Systems have a faulty weld that may result in oil leakage.
Recommended Action
Per FDA guidance
Customers were sent notification letters.
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 noticeDistribution
As reported by FDA
OR, VA
Page updated: Jan 10, 2026