AGFA recalls
AGFA has 11 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 30 Jul 2014.
Total recalls11since 2012
Last 12 months0reported
Class I00% of total
Ongoing0latest 30 Jul 2014
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 11 100%Class III 0 0%
Why agfa is recalled
Product types
By year
All agfa recalls, newest first
11 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Digital Radiography X-Ray system Dx-d 100 Agfa's Dx-d recalled | AGFA | Other | Nationwide |
| Device | CLASS II | Impax CV Pediatric Echo Reporting recalled by AGFA | AGFA | Device Malfunction | SC |
| Device | CLASS II | Impax Ris Qdoc recalled by AGFA | AGFA | Other | 9 states |
| Device | CLASS II | Impax 2 DB Server (running Oracle 1.0.4.0) recalled by AGFA | AGFA | Device Malfunction | Nationwide |
| Device | CLASS II | Digital Radiography X-Ray System Dx-d 100 Agfa's Dx-d recalled | AGFA | Other | Nationwide |
| Device | CLASS II | Impax CV Reporting Cardiac Catheterization module recalled by AGFA | AGFA | Other | Nationwide |
| Device | CLASS II | Impax CV 8 SU3 - OCR Service recalled by AGFA | AGFA | Device Malfunction | FL, KY |
| Device | CLASS II | CR MD1.0 General Set, x-ray imager image plate recalled by AGFA | AGFA | Other | Nationwide |
| Device | CLASS II | Impac CV DICOMStore with Media Purge Daemon (Mpd) recalled by AGFA | AGFA | Other | Nationwide |
| Device | CLASS II | Impax Cardiovascular (CV) Reporting Reporting tool used recalled by AGFA | AGFA | Other | Nationwide |
About this list
Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.