Device recall
Z-0387-06: LOCIQ Book System models: 2399921, 2399923, 2349933, 2349934 and 2349935
FDA device recall · Class II · General Electric Med Systems LLC
Key facts
| Recall number (Z-number) | Z-0387-06 |
|---|---|
| Recall event | 33266 |
| Product | LOCIQ Book System models: 2399921, 2399923, 2349933, 2349934 and 2349935 |
| Product code | IYN |
| Recalling firm | General Electric Med Systems LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 5, 2007 |
| 510(k) numbers | K014206 |
| FEI number | 2126677 |
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