Eos Imaging Inc: Medical Device Recall in 2012 - (Recall #: Z-2072-2012)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2012.

Data Source: FDA.

Product Description:

EOS X-ray Medical Diagnostic , X-ray Equipment System Digital Radiography used in general radiographic examination.

Product Classification:

Class II

Date Initiated: June 19, 2012

Date Posted: October 10, 2012

Recall Number: Z-2072-2012

Event ID: 62621

Reason for Recall:

It was discovered of several generator failures of the EOS System due to failure of its anode controller board that drives the rotation of the X-ray tube anode.

Status: Terminated

Product Quantity: 12 EOS Systems installed in the US

Code Information:

All associated Serial Numbers

Distribution Pattern:

Nationwide distribution

Voluntary or Mandated:

Voluntary: Firm initiated