Device recall
Z-0431-2013: Styker Orthobiologics Vita Plasma Separator, a component of Vitagel Surgical…
FDA device recall · Class II · Stryker Orthobiologics, Inc.
Key facts
| Recall number (Z-number) | Z-0431-2013 |
|---|---|
| Recall event | 62834 |
| Product | Styker Orthobiologics Vita Plasma Separator, a component of Vitagel Surgical Hemostat. Sterile, single use device designed to prepare plasma from the patient's blood using a tabletop centrifuge. |
| Product code | LMF |
| Recalling firm | Stryker Orthobiologics, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 29, 2014 |
| PMA numbers | P050044 |
| FEI number | 1000307073 |
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