Stryker Instruments Div. of Stryker Corporation: Medical Device Recall in 2014 - (Recall #: Z-1715-2014)

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:

The Stryker NAV3i Platform is a mobile cart platform consisting of the sub-components Stryker Nav3 Graphite Camera, SPC-3 Computer and IO-Tablet (touch screen) as well as the monitor, articulated arms and cart housing. This Navigation system is used in combination with surgical software for cranial, spine, ENT, orthopedic and trauma procedures.

Product Classification:

Class II

Date Initiated: May 13, 2014

Date Posted: June 11, 2014

Recall Number: Z-1715-2014

Event ID: 68261

Reason for Recall:

The Stryker NAV3i Platform Power Boxes produced between December 9, 2013 and March 7, 2014 may have been assembled without electrical insulation of the soldering joints

Status: Terminated

Product Quantity: 20

Code Information:

Stryker Product Number: 7700-800-000 Stryker Serial Numbers: 15097, 15098, 15099, 15102, 15103, 15104, 15105, 15106, 15107, 15109, 15110, 15111, 15112, 15113, 15114, 15115, 15116, 15117, 15118

Distribution Pattern:

Distributed in the states of AR, CA, IN, LA, MA, MD, MI, MT, NV, and TX.

Voluntary or Mandated:

Voluntary: Firm initiated