Device recall
Z-1287-2016: NecLoc Extrication Collar Product Usage: Necloc collars are applied to patients…
FDA device recall · Class II · Ossur H / F
Key facts
| Recall number (Z-number) | Z-1287-2016 |
|---|---|
| Recall event | 73380 |
| Product | NecLoc Extrication Collar Product Usage: Necloc collars are applied to patients afflicted with cervical injuries to ensure immobilization. |
| Product code | IQK |
| Recalling firm | Ossur H / F |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 15, 2016 |
| FEI number | 3003764610 |
At a glance
- None Linked 510(k)s
- 10–99 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