Eos Imaging Inc: Medical Device Recall in 2015 - (Recall #: Z-1460-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product Description:

EOS, Digital radiography system used in general radiographic examinations.

Product Classification:

Class II

Date Initiated: February 17, 2015

Date Posted: May 13, 2015

Recall Number: Z-1460-2015

Event ID: 70732

Reason for Recall:

When performing calibration, an alert message on the spectral filtration of the X-ray beam may be suppressed. Improper filtration of the X-ray Beam can then occur in exams set up with copper filtration.

Status: Terminated

Product Quantity: 13 units installed in US

Code Information:

Model Number - EOS System

Distribution Pattern:

US Distribution to the states of: CA, DE, PA, MN, FL, MO, OH, IN and IL.

Voluntary or Mandated:

Voluntary: Firm initiated