Device recall
Z-0845-2011: Micrus Endovascular Microcoil Delivery System; The Micrus Microcoil Delivery…
FDA device recall · Class II · Micrus Endovascular Corp., 821 Fox Lane, San Jose, CA 95131
Key facts
| Recall number (Z-number) | Z-0845-2011 |
|---|---|
| Recall event | 57192 |
| Product | Micrus Endovascular Microcoil Delivery System; The Micrus Microcoil Delivery System consists of three components, a Microcoil System, a Connecting Cable, and a Detachment Control Box (DCB). Each component is sold separately. Catalog Numbers: PC4180933, SSR181128, CPL100252, PC4181647, SSR181640… |
| Product code | HCG |
| Recalling firm | Micrus Endovascular Corp., 821 Fox Lane, San Jose, CA 95131 |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 11, 2011 |
| 510(k) numbers | K062036, K072173, K083646 |
| FEI number | 3003079393 |
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