Toshiba American Med Sys Inc Toshiba Digital Radiography System Model DFP8000D Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Toshiba Digital Radiography System Model DFP8000D
Brand
Toshiba American Med Sys Inc
Lot Codes / Batch Numbers
Serial #s W1C0552175, W1C0552181, W1C0562189
Products Sold
Serial #s W1C0552175, W1C0552181, W1C0562189
Toshiba American Med Sys Inc is recalling Toshiba Digital Radiography System Model DFP8000D due to In certain conditions the FOV of the lateral plane does not coincide with the X-ray exposed area, and consequently a part of the X-ray field may not b. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
In certain conditions the FOV of the lateral plane does not coincide with the X-ray exposed area, and consequently a part of the X-ray field may not be displayed in the magnification mode.
Recommended Action
Per FDA guidance
An Advisory Letter will be sent to customers via certified mail. Corrected software will be provided at no charge. Customers can contact their local Toshiba Service person to schedule the software update.
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
CO, MI, TX
Page updated: Jan 10, 2026