The NAV3i Platform Power Box supplies the electrical components with… — Class II medical device recall Z-1716-2014
Terminated recall by Stryker Instruments Div. of Stryker Corporation, reported 2014-06-11, distributed in AR, CA, IN, LA, MA, MD, MI, MT…. The Stryker NAV3i Platform Power Boxes produced between December 9, 2013 and March 7, 2014 may have been assem
| Recall number | Z-1716-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Stryker Instruments Div. of Stryker Corporation, Portage, MI, United States |
| Recall initiated | 2014-05-13 |
| Classified | 2014-06-04 |
| Reported by FDA | 2014-06-11 |
| Terminated | 2014-09-15 |
| Distributed | AR, CA, IN, LA, MA, MD, MI, MT, NV, TX |
| Quantity | 20 |
| Serial numbers | 10004 |
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 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
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1716-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.