Neptune 2 Rover Ultra Waste Management System — Class II medical device recall Z-0902-2014
Terminated recall by Stryker Instruments Div. of Stryker Corporation, reported 2014-02-12, distributed nationwide. The purpose of this correction is to upgrade the Neptune 2 Waste Management Systems in the field to the recent
| Recall number | Z-0902-2014 |
|---|---|
| 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 | 2013-12-30 |
| Classified | 2014-01-31 |
| Reported by FDA | 2014-02-12 |
| Terminated | 2016-01-12 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, CA, DE, NZ |
| Model numbers | 0702-001-000 |
Product
Neptune 2 Rover Ultra Waste Management System.
Reason for recall
The purpose of this correction is to upgrade the Neptune 2 Waste Management Systems in the field to the recently obtained 510(k) clearance specifications.
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-0902-2014. 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.