GE OEC Medical Systems, Inc: Medical Device Recall in 2017 - (Recall #: Z-1060-2017)

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 9900 Elite. MDL Numbers: D148942, D155043

Product Classification:

Class II

Date Initiated: December 27, 2016

Date Posted: February 1, 2017

Recall Number: Z-1060-2017

Event ID: 76074

Reason for Recall:

GE Healthcare Surgery announces a voluntary field action for the OEC 9800 and OEC 9900 Elite due to additional supplementation to the user documentation to include areas for enhanced planned maintenance and component replacement frequencies.

Status: Terminated

Product Quantity: 26,256 total

Code Information:

Manufactured from Oct 2005 to present

Distribution Pattern:

Worldwide including govt/VA/military and foreign consignees.

Voluntary or Mandated:

Voluntary: Firm initiated