AGFA Healthcare Corp.: Medical Device Recall in 2014 - (Recall #: Z-2176-2014)

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:

Agfa Digital Radiography X-Ray System DX-D 100 Product Usage: Is indicated for use in providing diagnostic quality images to aid the physician with diagnoses.

Product Classification:

Class III

Date Initiated: May 13, 2014

Date Posted: August 20, 2014

Recall Number: Z-2176-2014

Event ID: 68798

Reason for Recall:

Unit was mislabeled with a factory label showing 32 KW output power.

Status: Terminated

Product Quantity: 1

Code Information:

Serial Number A5410000042

Distribution Pattern:

US in the state of WV

Voluntary or Mandated:

Voluntary: Firm initiated