Drug recall
Mizuho Sugita Titanium Standard Aneurysm Clip II, Temporary and permanent occlusion of cervical segment of…
FDA recall event 66561 · Class II · Mizuho America, Inc.
Key facts
| Event ID | 66561 |
|---|---|
| Recall numbers | Z-0377-2014, Z-0378-2014 |
| Recalling firm | Mizuho America, Inc. |
| Product type | Devices |
| Products | 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., 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… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Specific item numbers form Lots 27-J and 29-J of Sugita T2 Aneurysm Clips. Mini Temporary Type, are discolored. |
| Initiation date | Oct 10, 2013 |
| Report date | Dec 4, 2013 |
| Termination date | Jan 13, 2014 |
| City | Union City |
| State | CA |
| Country | United States |
| FEI number | 1000159388 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: