Device recall
Z-2161-2016: Target Detachable Coils: TARGET 360 NANO 1 MM X 3 CM MODEL Number: M0035421030…
FDA device recall · Class II · Stryker Neurovascular
Key facts
| Recall number (Z-number) | Z-2161-2016 |
|---|---|
| Recall event | 74425 |
| Product | Target Detachable Coils: TARGET 360 NANO 1 MM X 3 CM MODEL Number: M0035421030 Neurology: Target Detachable Coils are intended to endovascularly obstruct or occlude blood flow in vascular abnormalities of the neurovascular and peripheral vessels. |
| Product code | HCG |
| Recalling firm | Stryker Neurovascular |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 3, 2017 |
| 510(k) numbers | K113412, K153658 |
| FEI number | 3008853977 |
At a glance
- 1–9 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