Class II — Mizuho America, Inc.
| Recalling firm | MIZUHO AMERICA, INC. |
|---|---|
| Registered facility | MIZUHO AMERICA, INC. (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Specific item numbers form Lots 27-J and 29-J of Sugita T2 Aneurysm Clips. Mini Temporary Type, are discolored. |
| Product | Mizuho Sugita Titanium Standard Aneurysm Clip II , Temporary Mini Type No 58 Temporary and permanent occlusion of cervical segment of cerebral aneurysms and peripheral blood vessels. They are designed for Single Use. |
| Quantity | 35 |
| Distribution | Nationwide Distribution |
| Initiated | 2013-10-10 |
| Classified | 2013-11-22 |
| Terminated | 2014-01-13 |
| Recall number | Z-0378-2014 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Mizuho America, Inc. (Z-0378-2014).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/66561/
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