Philips Medical Systems, Inc.: Medical Device Recall in 2014 - (Recall #: Z-1503-2014)

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:

Digital Diagnost, stationary radiographic system; Models: 712020/22/25/26/50/52/54/55/57/60/62/80/81/82/85

Product Classification:

Class II

Date Initiated: March 17, 2014

Date Posted: April 30, 2014

Recall Number: Z-1503-2014

Event ID: 67859

Reason for Recall:

The footboard of Patient support for stitching can be fixed in upper position. When the fix clamp (hook) is not correctly adjusted into its correct position, the footboard is not securely held.

Status: Terminated

Product Quantity: 985 devices

Code Information:

Units distributed from November 2006 through March 2014.

Distribution Pattern:

Nationwide: US: AL, AR, AZ, CA, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, MA, MD, ME, MN, MO, MS, MT, NC, ND, NH, NJ, NM, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VT, WY / Worldwide including Canada & Mexico

Voluntary or Mandated:

Voluntary: Firm initiated