Device recall
Z-0270-2016: Stryker Radius 5.5 to 3.5 Rod to Red Connector, REF 48664530. Intended to…
FDA device recall · Class II · Stryker Spine
Key facts
| Recall number (Z-number) | Z-0270-2016 |
|---|---|
| Recall event | 72413 |
| Product | Stryker Radius 5.5 to 3.5 Rod to Red Connector, REF 48664530. Intended to provide additional support during fusion using autograft or allograft in skeletally mature patients. |
| Product code | NKB |
| Recalling firm | Stryker Spine |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 26, 2016 |
| FEI number | 3004024955 |
At a glance
- None 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