Philips Medical Systems, Inc.: Medical Device Recall in 2013 - (Recall #: Z-0431-2014)

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:

Easy Diagnost Eleva Universal Fluoroscopic applications

Product Classification:

Class II

Date Initiated: October 30, 2013

Date Posted: December 11, 2013

Recall Number: Z-0431-2014

Event ID: 66705

Reason for Recall:

The delivered application software was an outdated version to the model of equipment.

Status: Terminated

Product Quantity: 19 devices

Code Information:

706050, 706083, 706088

Distribution Pattern:

Nationwide Distribution including MN, NH, DE, OR, MA, TX, OH, FL, CA, WA, and SC.

Voluntary or Mandated:

Voluntary: Firm initiated