RecallRadar

FDA Device recall Z-1716-2014

The NAV3i Platform Power Box supplies the electrical components with power (e.g. Stryker Nav3 Graphite Camera, SPC-3 Computer, IO-Tablet (t…

On 2014-06-11 the FDA classified a Class II recall of The NAV3i Platform Power Box supplies the electrical components with power (e.g. Stryker Nav3 Graphite Camera, SPC-3 Computer, IO-Tablet (t… by Stryker Instruments Div, citing 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.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-1716-2014
ClassificationClass II
Statusterminated
Initiated2014-05-13
Published2014-06-11
Last updated2026-09-13 11:53 UTC
CompanyStryker Instruments Div
DistributionAR, CA, IN, LA, MA, MD, MI, MT, NV, TX

Product

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).

Reason

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

Identifiers

code_infoStryker Product Number: 7700-853-000 Stryker Serial Numbers: 10004

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1716-2014%22

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