AGFA Healthcare Corp.: Medical Device Recall in 2014 - (Recall #: Z-2175-2014)

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:

DX-D 600 - DXD Imaging Package Product Usage:Is indicated for use in providing diagnostic quality images to aid the physician with diagnosis. Systems can be used with MUSICA2 image processing to create radiographic images of the skeleton including skull, spinal column and extremities, check abdomen and other both parts.

Product Classification:

Class II

Date Initiated: July 2, 2014

Date Posted: August 20, 2014

Recall Number: Z-2175-2014

Event ID: 68752

Reason for Recall:

Some customers reported that while using the DX-D600 in room or exam preparation, the Overhead Tube Crane (OTC) showed increased velocity and uncontrolled longitudinal movement.

Status: Terminated

Product Quantity: 17 units

Code Information:

Serial Nos. A5430000089, A5430000131, A5430000015, A5430000095, A5430000052, A5430000061, A5430000079, A5430000030, A5430000042, A5430000066, A5430000081, A5430000085, A5430000096, A5430000020, A5430000067, A5430000125, A5430000105

Distribution Pattern:

Worldwide Distribution - US Natinwide in the state of GA, IN, KS, KY, MA, NJ, SC, VA, DC and the country of Canada

Voluntary or Mandated:

Voluntary: Firm initiated