Philips Electronics North America Corporation: Medical Device Recall in 2017 - (Recall #: Z-2154-2017)

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:

Philips DigitalDiagnost 3.1.x X-Ray System

Product Classification:

Class II

Date Initiated: May 11, 2017

Date Posted: June 21, 2017

Recall Number: Z-2154-2017

Event ID: 77312

Reason for Recall:

During recent evaluations of the Philips DigitalDiagnost 3.1.x, we have identified a potential issue that may affect the performance of the equipment under certain conditions.

Status: Terminated

Product Quantity: US - 132

Code Information:

DigitalDiagnost Upgrade Release 3.1.x to 3.1.3

Distribution Pattern:

USA(nationwide) Distribution to the states of : AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, IL, IN, KY, LA, MA, ME, MI, MN, MO, NC, ND, NE, NH, NM, NY, OH, OK, OR, PA, TN, TX, UT, VA, WA and WI

Voluntary or Mandated:

FDA Mandated