co_sos
1 records
EPA (Environmental Protection Agency)
2 records
epa_echo
2 records
EPA ECHO: AGFA CORPORATION
1991-02-22
Penalty assessed: $117,725. Type: Administrative - Formal
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fda
10 records
FDA Recall: AGFA Corp. — Class II
20140730
When liquid comes in contact with the DX-D 100 touch screen, the device may incorrectly recognize this as user input altering device settings. | Product: AGFA Digital Radiography X-Ray system DX-D 100...
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FDA Device Recall: AGFA Digital Radiography X-Ray system DX-D 100 Agfa's DX-D 100 is indicated f
2014-07-30
Class II — When liquid comes in contact with the DX-D 100 touch screen, the device may incorrectly recognize this as user input altering device settings.
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FDA Device Recall: IMPAX CV Pediatric Echo Reporting, IMPAX CV Echo Measurement Import via Optical
2014-06-04
Class II — Failure to effectively install and test a hotfix to correct the known software defect within the IMPAX CV 7.8 SU3-OCR Service.
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FDA Device Recall: IMPAX RIS QDOC 5.8
2014-02-12
Class II — Patient name displayed (printed) on the Patient Report was the wrong patient name.
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FDA Recall: AGFA Corp. — Class II
20130417
Software design error in IMPAX CV 7.8 SU3 | Product: IMPAX CV 7.8 SU3 - OCR Service. The IMPAX CV Reporting component facilitates the quick , effectiv
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FDA Device Recall: IMPAX 5.2 DB Server (running Oracle 10.1.0.4.0), medical imaging Picture Archivi
2013-10-30
Class II — System downtime and/or slow performance may result if software in use is an old version of IMPAX and is not at current supported levels.
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FDA Device Recall: IMPAX CV 7.8 SU3 - OCR Service. The IMPAX CV Reporting component facilitates
2013-04-17
Class II — Software design error in IMPAX CV 7.8 SU3
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FDA Device Recall: CR MD1.0 General Set, x-ray imager image plate. CR 10-X Image Plate 35CM X 43CM
2013-03-27
Class II — The cassettes were shipped with the wrong IP (image plate) size bar code.
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FDA Device Recall: AGFA IMPAC CV DICOMStore with Media Purge Daemon (MPD) and IMPAX CV DICOMStore
2012-08-29
Class II — Loss of patient data can occur under certain circumstances due to misconfiguration of DICOMstore configured with Agfa's Medical Image Storage Devices - Media Purge Daemon (MPD) and Cardiova...
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FDA Device Recall: IMPAX Cardiovascular (CV) Reporting Reporting tool used for structured report
2012-08-22
Class II — Content entered into the "Conclusions" free text box on the Report Writer screen was not represented on the final printed report.
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ny_corps
1 records
NY Corp: AGFA CORPORATION
1998-11-25
FOREIGN BUSINESS CORPORATION | County: New York | Jurisdiction: Delaware
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