FDA Device recall Z-0903-2014
Neptune 2 Rover Ultra Waste Management System
- FDA Device
- Class II
- terminated
- Published 2014-02-12
On 2014-02-12 the FDA classified a Class II recall of Neptune 2 Rover Ultra Waste Management System by Stryker Instruments Div, citing 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.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0903-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-12-30 |
| Published | 2014-02-12 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Stryker Instruments Div |
| Distribution | US |
Product
Neptune 2 Rover Ultra Waste Management System
Reason
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.
Identifiers
| code_info | Manufacturer Part Number 0702-002-000 (230V) All serial numbers |
|---|
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-0903-2014%22
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