Device recall
Z-2772-2015: Aliquot Delivery Kit (Syringe and Plunger); for use in open and percutaneous…
FDA device recall · Class II · Orthovita, Inc., dBA Stryker Orthobiologics.
Key facts
| Recall number (Z-number) | Z-2772-2015 |
|---|---|
| Recall event | 72054 |
| Product | Aliquot Delivery Kit (Syringe and Plunger); for use in open and percutaneous procedures to facilitate placement of bone cement in weakened or diminished bone |
| Product code | KIH |
| Recalling firm | Orthovita, Inc., dBA Stryker Orthobiologics. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 10, 2017 |
| FEI number | 1000307073 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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