AGFA Corp.: Medical Device Recall in 2012 - (Recall #: Z-2252-2012)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2012.

Data Source: FDA.

Product Description:

AGFA IMPAC CV DICOMStore with Media Purge Daemon (MPD) and IMPAX CV DICOMStore with Cardiovascular Purge Services (CPS), Medical Image Storage Device

Product Classification:

Class II

Date Initiated: August 9, 2012

Date Posted: August 29, 2012

Recall Number: Z-2252-2012

Event ID: 62796

Reason for Recall:

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 Cardiovascular Purge Service (CPS).

Status: Terminated

Product Quantity: 535

Code Information:

All software versions of DICOMstore in combination with Media Purge Daemon (MPD) or Cardiovascular Purge Services (CPS).

Distribution Pattern:

USA Nationwide, Virgin Islands and Canada

Voluntary or Mandated:

Voluntary: Firm initiated