Device recall
Z-0761-2007: Bio-logic-Ceegraph/Sleepscan Netlink Traveler, Bio-logic Systems Corp., a nebus…
FDA device recall · Class II · Bio-Logic Systems Corp
Key facts
| Recall number (Z-number) | Z-0761-2007 |
|---|---|
| Recall event | 37518 |
| Product | Bio-logic-Ceegraph/Sleepscan Netlink Traveler, Bio-logic Systems Corp., a nebus company, Mundelein, IL 60060; Model 580-T2ASM2. (a Digital EEG/Sleep Recorder Electroencephalograph that includes a built-in pulse oximeter, body position sensor, snore monitor, chest, abdominal and air flow transducers… |
| Product code | GWQ |
| Recalling firm | Bio-Logic Systems Corp |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 26, 2008 |
| 510(k) numbers | K052066 |
| FEI number | 1419887 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 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