AGFA Corp.: Medical Device Recall in 2013 - (Recall #: Z-1487-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

Product Description:

AGFA Digital Radiography X-Ray System DX-D 100 Agfa's DX-D 100 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: chest, abdomen, and other body parts.

Product Classification:

Class II

Date Initiated: May 15, 2013

Date Posted: June 12, 2013

Recall Number: Z-1487-2013

Event ID: 65223

Reason for Recall:

Customers could potentially experience intermittent, unintended and illogical movement when using the product.

Status: Terminated

Product Quantity: 104

Code Information:

Material numbers in US - 5Q82F, 5R75Q, 5Q8ZB, 5R77U & 58Q1D - Material numbers in Canada - 5R78W & 5R77U

Distribution Pattern:

Worldwide Distribution - US Nationwide including the states of AL, FL, IL, IN, IA, KY, MA, MI, MN, MS, MO, NE, NJ, NY, NC, OH, OR, SC, TN, VA, WV, WY and the country of Canada

Voluntary or Mandated:

Voluntary: Firm initiated