Device recall
Z-1390-2013: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument…
FDA device recall · Class II · Orthovita, Inc., dBA Stryker Orthobiologics.
Key facts
| Recall number (Z-number) | Z-1390-2013 |
|---|---|
| Recall event | 63204 |
| Product | Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument - Aliquot Syringe Delivery System, 6", Part Number 2090-0504 Product Usage: Facilitate placement of bone cement in weakened or diminished bone |
| Product code | OAR |
| Recalling firm | Orthovita, Inc., dBA Stryker Orthobiologics. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 29, 2014 |
| FEI number | 1000307073 |
At a glance
- None Linked 510(k)s
- 10–99 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