GE OEC Medical Systems, Inc: Medical Device Recall in 2017 - (Recall #: Z-1469-2017)

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:

OEC FlexiView 8800, Digital Mobile Imaging System, GE Medical Systems

Product Classification:

Class II

Date Initiated: February 21, 2017

Date Posted: March 22, 2017

Recall Number: Z-1469-2017

Event ID: 76568

Reason for Recall:

OEC FlexiView 8800 workstation power cable assembly issue which can result in a loss of imaging functionality due to intermittent power cord failures.

Status: Terminated

Product Quantity: 1

Code Information:

OEC FlexiView 8800 systems that had NEMA 5-15 15 Amp power cords replaced between January 28, 2016 and November 23, 2016.

Distribution Pattern:

One consignee in CA.

Voluntary or Mandated:

Voluntary: Firm initiated