Philips Electronics North America Corporation: Medical Device Recall in 2016 - (Recall #: Z-0375-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

Philips Healthcare System X-ray Tomography Computed :

Product Classification:

Class II

Date Initiated: March 15, 2016

Date Posted: November 30, 2016

Recall Number: Z-0375-2017

Event ID: 75551

Reason for Recall:

It was discovered the patient support tabletop may fail to move in the horizontal direction when it is commanded to do so during CT scans due to a potential mechanical linkage failure.

Status: Terminated

Product Quantity: 1363

Code Information:

Brilliance iCT SP, Brilliance iCT, Brilliance 64, Brilliance 40, Brilliance 16, Brilliance 16P, Brilliance 10, Brilliance 6, Brilliance Big Bore.

Distribution Pattern:

USA(nationwide) Distribution to the states of : AZ, NY, GA, UT, TN, TX, AR, NV, Il, FL, MS, LA, MD, MO, MA, OK, KY, WY, SC, ND, NE, DE, MI, WA, CT, RI, KS, OR, IN, PA, CA, NJ, NC, MN, AL and IA.

Voluntary or Mandated:

FDA Mandated