AGFA Corp. Recalls

Overview of recall records associated with AGFA Corp., including dates, categories and classifications where available.

2recall records

Jul 30, 2014latest record date

Jun 4, 2014earliest record date

Recall history in this database

Classification mix: Class II: 2.

Medical DeviceJul 30, 2014

AGFA Digital Radiography X-Ray system DX-D 100 Agfa's DX-D 100 is indicated for use in recall — FDA Z-2081-2014

When liquid comes in contact with the DX-D 100 touch screen, the device may incorrectly recognize this as user input altering device settings.

Class IIFDA: TerminatedAGFA Corp.

Medical DeviceJun 4, 2014

AGFA IMPAX CV Pediatric Echo Reporting, IMPAX CV Echo Measurement Import via Optical recall — FDA Z-1662-2014

Failure to effectively install and test a hotfix to correct the known software defect within the IMPAX CV 7.8 SU3-OCR Service.

Class IIFDA: TerminatedAGFA Corp.

Understanding this recall history

This page summarizes recall records in which the official source identifies AGFA Corp. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.

Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.