Device recall
Z-1553-2009: Cyberkinetics Inserter Wand & V2 Trigger Assembly, Expiration: July 14, 2009…
FDA device recall · Class II · Cyberkinetics Neurotechnology Systems, Inc.
Key facts
| Recall number (Z-number) | Z-1553-2009 |
|---|---|
| Recall event | 51951 |
| Product | Cyberkinetics Inserter Wand & V2 Trigger Assembly, Expiration: July 14, 2009; Catalog Number: 4468. |
| Product code | GZL |
| Recalling firm | Cyberkinetics Neurotechnology Systems, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 20, 2009 |
| 510(k) numbers | K042384 |
| FEI number | 3005346158 |
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