FDA Recall Terminated

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.

Recall: Z-2056-2019 · Initiated June 27, 2019

Recall

Recall Number
Z-2056-2019
Event Number
83400
Firm
Agfa N.V. Septestraat 27 Mortsel Belgium
FEI Number
3001556265
Product Code
JAA
Status
Terminated
Root Cause
Device Design
Initiated
June 27, 2019
Terminated
June 3, 2020

Description

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

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

Action

The firm sent notification letter dated June 27, 2019 to affected customers. The letter identified the affected product problem and actions to be taken. For questions about this matter,contact your local Agfa Imaging organization 1-877-777-2432 and please reference Problem Record. PRB2000198.

Distribution

US Nationwide Distribution

Quantity

4