Agfa N.V. Septestraat 27 Mortsel Belgium AGFA Digital Radiography X- Ray system DR 800 with TomoSynthesis- a Tomographic X-ray system - Product Usage: TomoSynthesis is used to synthesize tomographic slices from a single tomographic sweep. The DR 800 is not intended for mammography applications Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
AGFA Digital Radiography X- Ray system DR 800 with TomoSynthesis- a Tomographic X-ray system - Product Usage: TomoSynthesis is used to synthesize tomographic slices from a single tomographic sweep. The DR 800 is not intended for mammography applications
Brand
Agfa N.V. Septestraat 27 Mortsel Belgium
Lot Codes / Batch Numbers
Serial Numbers: 00949, 1161
Products Sold
Serial Numbers: 00949, 1161
Agfa N.V. Septestraat 27 Mortsel Belgium is recalling AGFA Digital Radiography X- Ray system DR 800 with TomoSynthesis- a Tomographic X-ray system - Produ due to Tomosynthesis image acquisition sequence did not stop automatically after expected number of exposures.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Tomosynthesis image acquisition sequence did not stop automatically after expected number of exposures.
Recommended Action
Per FDA guidance
AFGA issued via email On February 10, 2020, an URGENT FIELD SAFETY NOTICE letter. Letter states reason for recall, health risk, and action to take: With this letter, Agfa is informing you that the DR 800 system still can be used including for Tomosynthesis for mAs values which are larger than 0,2 mAs. In case Tomosynthesis image acquisition sequence does not stop automatically after the expected number of exposures, release the exposure button as this will stop the sequence and notify your Agfa Service contact at once. Contact your local Agfa Imaging organization 1-877-777-2432 and please reference Problem Record PRB2000387 and Vigilance Record VR0000716. Complete/Return by fax or email the URGENT FIELD SAFETY NOTICE Feedback form
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