120 V Neptune 3 Rover — Class II medical device recall Z-2630-2016
Terminated recall by Stryker Instruments Div. of Stryker Corporation, reported 2016-08-31, distributed in CA, IA, ID, MI, VA. Stryker initiated a voluntary recall of the 120 V Neptune 3 Rover on 07/01/2016, due to a potential for the de
| Recall number | Z-2630-2016 |
|---|---|
| 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 | 2016-07-01 |
| Classified | 2016-08-23 |
| Reported by FDA | 2016-08-31 |
| Terminated | 2017-06-02 |
| Distributed | CA, IA, ID, MI, VA |
| Quantity | 78 |
| Serial numbers | 1606300523, 1606300553, 1606300583, 1606300593, 1606300613, 1606300623, 1606300643, 1606300653, 1607503463, 1607503493, 1610409473, 1610606263, 1610606273, 1610606303, 1610606323, 1610606353, 1610619473, 1610619483, 1610619543, 1610619573, 1610619603, 1610903893, 1610903973, 1610904063, 1610904083 and 49 more |
| Model numbers | 0703-001-000 |
Product
120 V Neptune 3 Rover, Model Number: 0703-001-000
Reason for recall
Stryker initiated a voluntary recall of the 120 V Neptune 3 Rover on 07/01/2016, due to a potential for the device to experience system errors causing the device to shutdown if high levels of electromagnetic interference are present in the operating room.
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-2630-2016. 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.