Device recall
Z-0377-2014: Mizuho Sugita Titanium Standard Aneurysm Clip II, Temporary and permanent…
FDA device recall · Class II · Mizuho America, Inc.
Key facts
| Recall number (Z-number) | Z-0377-2014 |
|---|---|
| Recall event | 66561 |
| Product | Mizuho Sugita Titanium Standard Aneurysm Clip II , Temporary and permanent occlusion of cervical segment of cerebral aneurysms and peripheral blood vessels. They are designed for Single Use. |
| Product code | HCH |
| Recalling firm | Mizuho America, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 13, 2014 |
| 510(k) numbers | K990202 |
| FEI number | 1000159388 |
At a glance
- 1–9 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