Device recall
Z-0938-2015: Stryker Orthobiologics Imbibe Bone Marrow Aspiration Needle, Model Numbers…
FDA device recall · Class II · Orthovita, Inc., dBA Stryker Orthobiologics.
Key facts
| Recall number (Z-number) | Z-0938-2015 |
|---|---|
| Recall event | 69979 |
| Product | Stryker Orthobiologics Imbibe Bone Marrow Aspiration Needle, Model Numbers: 2090-0027 Needle (bullet-tip), 11 gauge x 4 inch 2090-0028 Needle (bullet-tip), 11 gauge x 6 inch 2090-0029 Needle (bullet-tip), 8 gauge x 6 inch 2090-0047 Needle (bullet-tip), 8 gauge x 8 inch 2090-0030 Needle (bullet-tip)… |
| Product code | KNW |
| Recalling firm | Orthovita, Inc., dBA Stryker Orthobiologics. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 28, 2015 |
| 510(k) numbers | K140414 |
| FEI number | 1000307073 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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