Device recall
Z-2212-2013: Zeppessis' reprocessed single-use manifolds (filters) for the Stryker Neptune 1…
FDA device recall · Class II · Zeppessis Reprocessing, LLC
Key facts
| Recall number (Z-number) | Z-2212-2013 |
|---|---|
| Recall event | 66176 |
| Product | Zeppessis' reprocessed single-use manifolds (filters) for the Stryker Neptune 1 and Neptune 2 Waste Management Systems: The Neptune Waste management system is intended to be used in the Operating Room, Surgical Centers and Doctor's Offices to collect and dispose of surgical fluid waste as well as… |
| Product code | JCX |
| Recalling firm | Zeppessis Reprocessing, LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 8, 2013 |
| FEI number | 3009142112 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database