Toshiba American Med Sys Inc Digital Radiography System, model DFP-8000D Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Digital Radiography System, model DFP-8000D
Brand
Toshiba American Med Sys Inc
Lot Codes / Batch Numbers
All codes
Products Sold
All codes
Toshiba American Med Sys Inc is recalling Digital Radiography System, model DFP-8000D due to Defect in the mirroring unit.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Defect in the mirroring unit.
Recommended Action
Per FDA guidance
An advisory letter will be sent to all users 6/24/2004. An order was issued to correct the firmware problem.
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