Eastman Kodak Co KODAK DirectView DR 7100 System, Catalog # 133-6049. This is a digital radiology system. The major components are: operator console; digital imaging capture device; tilting table with floating top; ceiling-mounted x-ray tube; x-ray generator timing and distribution unit. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
KODAK DirectView DR 7100 System, Catalog # 133-6049. This is a digital radiology system. The major components are: operator console; digital imaging capture device; tilting table with floating top; ceiling-mounted x-ray tube; x-ray generator timing and distribution unit.
Brand
Eastman Kodak Co
Lot Codes / Batch Numbers
s/n DR71000121 and DR71000123.
Products Sold
s/n DR71000121 and DR71000123.
Eastman Kodak Co is recalling KODAK DirectView DR 7100 System, Catalog # 133-6049. This is a digital radiology system. The major due to Potential weld defect in the Overhead Tube Support assembly which connects the tube assembly to the telescoping arm. This could cause the tube assemb. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Potential weld defect in the Overhead Tube Support assembly which connects the tube assembly to the telescoping arm. This could cause the tube assembly to fall, injuring anyone near the unit.
Recommended Action
Per FDA guidance
Letters dated 10/20/2005 were hand carried by Kodak Field Service Reps. Kodak Field Engineers inspected units and found the two defective units (both in China).
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
FL, IN, KY, MI, NY, OH, PA, SC
Page updated: Jan 10, 2026