FDA recall Z-2056-2019

Agfa N.V. · Class II · device

Product

AGFA Digital Radiography X- Ray system DR 800 with MUSICA Dynamic Product Usage: The Agfa s DR 800 system is indicated for performing dynamic imaging examinations (fluoroscopy and/or rapid sequence) of the following an anatomies/procedures: positioning fluoroscopy procedures, gastro-intestinal examinations, urogenital tract examinations, and angiography. It is intended to replace fluoroscopic images obtained through image intensifier technology. In addition, the system is intended for project radiography of all body parts. The DR 800 is not intended for mammography applications.

Reason for recall

The exposed area of fluo exams possibly does not match the active area of the detector within specified limits.

Distribution

US Nationwide Distribution

Key facts

Status
Terminated
Initiation date
2019-06-27
Report date
2019-08-07
Termination date
2020-06-03
Voluntary/Mandated
FDA Mandated
Location
Mortsel, N/A, Belgium

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2056-2019