Device recall
Z-2425-2010: Integra NeuroSciences Implants, NeuroBalloon Catheter, Sterile/EO, Rx only…
FDA device recall · Class I · Integra LifeSciences Corp
Key facts
| Recall number (Z-number) | Z-2425-2010 |
|---|---|
| Recall event | 56190 |
| Product | Integra NeuroSciences Implants, NeuroBalloon Catheter, Sterile/EO, Rx only, single use, latex free: Catalog Number 7CBD10 |
| Product code | HAO |
| Recalling firm | Integra LifeSciences Corp |
| Recall class | Class I |
| Status | Terminated |
| Termination date | May 29, 2012 |
| FEI number | 1121308 |
At a glance
- None Linked 510(k)s
- 1–9 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