Philips Medical Systems, Inc.: Medical Device Recall in 2014 - (Recall #: Z-0182-2015)

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:

Philips Medical Systems Allura Xper FD20C with software version R8.2.O System Code: 722035. The Allura Xper FD series are intended for use on human patients to perform: Vascular, cardiovascular and neurovascular imaging applications, including diagnostic, interventional and minimally invasive procedures.

Product Classification:

Class II

Date Initiated: July 8, 2014

Date Posted: November 19, 2014

Recall Number: Z-0182-2015

Event ID: 68723

Reason for Recall:

Faulty Automatic Motion Controller (AMC), a problem in the Power On Self Test (POST) error handling was detected, can result in a hazardous movement of the C-arc. system.

Status: Terminated

Product Quantity: 2 units

Code Information:

Allura Xper Software version R8.2.0

Distribution Pattern:

Distributed in the states of IL, and TN, and the countries of Argentina , Australia, Belgium, Denmark, Egypt, France, Germany, Hong Kong, Italy, Japan, Korea, Republic of Netherlands, Norway, Saudi Arabia, Switzerland, United Kingdom, and Viet Nam.

Voluntary or Mandated:

Voluntary: Firm initiated