GE Healthcare, LLC: Medical Device Recall in 2018 - (Recall #: Z-0195-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

Centricity Universal Viewer with Cross Enterprise Display This impacts product versions 6.0 SP1 and higher.

Product Classification:

Class II

Date Initiated: August 30, 2018

Date Posted: October 24, 2018

Recall Number: Z-0195-2019

Event ID: 81297

Reason for Recall:

Remote comparison studies displayed may be associated with the wrong patient, without a caution icon present.

Status: Terminated

Product Quantity: 1

Code Information:

SYSTEM ID: 315470CPUWPV UDI #: 8406821038 00DE #: 2090255-001

Distribution Pattern:

Voluntary or Mandated:

Voluntary: Firm initiated