Agfa-Gevaert, N.V.: Medical Device Recall in 2019 - (Recall #: Z-0692-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

DX-D 600 DIRECT RADIOGRAPHY SYSTEM Product Usage: The DX-D 600 system is a ceiling mounted General Radiography X-Ray imaging system used in hospitals, clinics and medical practices by physicists, radiographers and radiologists to make, process and view static X-Ray radiographic images of the skeleton (including skull, spinal column and extremities), chest, abdomen and other body parts on adult, pediatric or neonatal patients.

Product Classification:

Class II

Date Initiated: December 4, 2018

Date Posted: January 16, 2019

Recall Number: Z-0692-2019

Event ID: 81780

Reason for Recall:

After an upgrade of the software of the Overhead Tube Crane, there were isolated cases in which the Overhead Tube Crane movement does not stop when the movement button is released. Instead of stopping while the movement button is released, the Tube Head Crane moves to the intended position.

Status: Terminated

Product Quantity: 10

Code Information:

Serial Numbers: A5430000015 A5430000020 A5430000030 A5430000042 A5430000052 A5430000061 A5430000066 A5430000067 A5430000079 A5430000081

Distribution Pattern:

US Nationwide Distribution in the states: IN, KS, MA, SC, and VA.

Voluntary or Mandated:

Voluntary: Firm initiated