Device recall
Z-1036-2026: Codman Microsensor Basic Kit. Catalog Number: 626631US. Use of the CODMAN…
FDA device recall · Class II · Integra LifeSciences Corp. (NeuroSciences)
Key facts
| Recall number (Z-number) | Z-1036-2026 |
|---|---|
| Recall event | 98091 |
| Product | Codman Microsensor Basic Kit. Catalog Number: 626631US. Use of the CODMAN MICROSENSOR Basic Kit is indicated when direct ICP monitoring is required. The kit is indicated for use in both subdural and intraparenchymal pressure monitoring applications only. |
| Product code | GWM |
| Recalling firm | Integra LifeSciences Corp. (NeuroSciences) |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K153347 |
| FEI number | 3003418325 |
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