Philips Healthcare Inc.: Medical Device Recall in 2017 - (Recall #: Z-1706-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

Mobile Diagnostic X-Ray System with Digital Panel

Product Classification:

Class II

Date Initiated: November 28, 2012

Date Posted: April 12, 2017

Recall Number: Z-1706-2017

Event ID: 64902

Reason for Recall:

When the operator moves an image to another view then the electronic marker might be placed at the wrong anatomical position in the resulting image.

Status: Terminated

Product Quantity: 220 systems

Code Information:

*** All units ***

Distribution Pattern:

Nationwide (AR, AZ, CA, DE, FL, GA, IA, IL, IN, KS, MD, MI, MN, NC, NM, NY, OH, OR, PA, SC, TX, VT, WI)

Voluntary or Mandated:

Voluntary: Firm initiated