FDA Recall Terminated

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.

Recall: Z-0377-2014 · Initiated October 10, 2013

Recall

Recall Number
Z-0377-2014
Event Number
66561
Firm
Mizuho America, Inc.
FEI Number
1000159388
Product Code
HCH
Status
Terminated
Root Cause
Process control
Initiated
October 10, 2013
Posted
November 22, 2013
Terminated
January 13, 2014
Address
30057 Ahern Ave, Union City, CA, 94587-1234

Description

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.

Reason

Specific item numbers form Lots 27-J and 29-J of Sugita T2 Aneurysm Clips. Mini Temporary Type, are discolored.

Action

Mizuho sent a Product Recall Notice dated October 10, 2013, to all affected customers. The letter identified the product, the problem, and the action to be taken by the customer. Customers were asked to verify serial number before opening package and conduct a physical examination of the product for discolored Clips from the affected lots. Customers were also asked to fill out the Confirmation of User Receipt, and return to Misuho America. If customers should find affed clips they were instructed to quarantine them an call Mizuho America Customer Service at 800-699-2547 for return instructions. The Clips will be exchanged at no charge. Customers were also asked to ensure that all appropriate persons within the Hospital have been notified of the Recall Notice. For questions regarding this recall call 510-324-4500, ext 122.

Distribution

Nationwide Distribution

Quantity

32