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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 66561

2 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
October 10, 2013
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Mizuho America, Inc.

Dossier provenance

Source snapshots represented here

  • openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
  • openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

2 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 2

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.

Z-0377-2014
Recall number
Z-0377-2014
Initiated
October 10, 2013
Classification
Class II
Status
Terminated
Recalling firm
Mizuho America, Inc.
Quantity
32

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Specific item numbers form Lots 27-J and 29-J of Sugita T2 Aneurysm Clips. Mini Temporary Type, are discolored.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

Product Code 17-001-56; Lot No. 27JY

Distribution pattern

Nationwide Distribution

device · product 2 of 2

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.

Z-0378-2014
Recall number
Z-0378-2014
Initiated
October 10, 2013
Classification
Class II
Status
Terminated
Recalling firm
Mizuho America, Inc.
Quantity
35

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Specific item numbers form Lots 27-J and 29-J of Sugita T2 Aneurysm Clips. Mini Temporary Type, are discolored.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

Product Code 17-001-58; Lot No. 29JY

Distribution pattern

Nationwide Distribution