Drug recall
Neptune 2 Rover Ultra Waste Management System
FDA recall event 67191 · Class II · Stryker Instruments Div. of Stryker Corporation
Key facts
| Event ID | 67191 |
|---|---|
| Recall numbers | Z-0902-2014, Z-0903-2014 |
| Recalling firm | Stryker Instruments Div. of Stryker Corporation |
| Product type | Devices |
| Products | Neptune 2 Rover Ultra Waste Management System, Neptune 2 Rover Ultra Waste Management System. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| 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. |
| Initiation date | Dec 30, 2013 |
| Report date | Feb 12, 2014 |
| Termination date | Jan 12, 2016 |
| City | Portage |
| State | MI |
| Country | United States |
| FEI number | 1811755 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: