Fischer Imaging Corporation VersaRad/Traumex General Radiographic System. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
VersaRad/Traumex General Radiographic System.
Brand
Fischer Imaging Corporation
Lot Codes / Batch Numbers
All units.
Products Sold
All units.
Fischer Imaging Corporation is recalling VersaRad/Traumex General Radiographic System. due to If two of the four T-nuts that connect the transverse rail to the ceiling rail fail, the 'U' arm and transverse rails could fall and cause serious inj. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
If two of the four T-nuts that connect the transverse rail to the ceiling rail fail, the 'U' arm and transverse rails could fall and cause serious injury.
Recommended Action
Per FDA guidance
Consignees were notified by letter on 4/23/2004.
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