Drug recall

The NAV3i Platform Power Box supplies the electrical components with power (e.g. Stryker Nav3 Graphite Camera…

FDA recall event 68261 · Class II · Stryker Instruments Div. of Stryker Corporation

Key facts

Event ID 68261
Recall numbers Z-1715-2014, Z-1716-2014
Recalling firm Stryker Instruments Div. of Stryker Corporation
Product type Devices
Products The NAV3i Platform Power Box supplies the electrical components with power (e.g. Stryker Nav3 Graphite Camera, SPC-3 Computer, IO-Tablet (touch screen) and the monitor)., 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…
Classification Class II
Status Terminated
Voluntary or mandated Firm Initiated
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
Initiation date May 13, 2014
Report date Jun 11, 2014
Termination date Sep 15, 2014
City Portage
State MI
Country United States
FEI number 1811755

At a glance

  • 1–9 Products in this recall
  • 10–99 FDA inspections of this firm (FEI)

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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