AGFA Corp.: Medical Device Recall in 2014 - (Recall #: Z-0919-2014)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

IMPAX RIS QDOC 5.8

Product Classification:

Class II

Date Initiated: January 8, 2014

Date Posted: February 12, 2014

Recall Number: Z-0919-2014

Event ID: 67275

Reason for Recall:

Patient name displayed (printed) on the Patient Report was the wrong patient name.

Status: Terminated

Product Quantity: 14

Code Information:

Software IMPAX RIS 58 and higher

Distribution Pattern:

CA, FL, GA, ME, OH, OR, SC, SD, TX and Canada

Voluntary or Mandated:

Voluntary: Firm initiated