Exact FDA event identifier

Event 68512

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

Event summary

Timeline bucket: May 28, 2014
Product types: Device
Classifications: Class II
Statuses: Terminated
Recalling firm wording: Vascular Technology, 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

4 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 4

07-150-07 MIZUHO, MAL DISP DOPPLER PROBE BX 4, REF 138200 The Doppler probe is intended for the intraoperative and transcutaneous evaluation of blood flow.

Z-1998-2014

Recall number: Z-1998-2014
Initiated: May 28, 2014
Classification: Class II
Status: Terminated
Recalling firm: Vascular Technology, Inc.
Quantity: 164

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

Report of the product penetrating the sterile barrier; this could render the product unsterile.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Report of the product penetrating the sterile barrier; this could render the product unsterile.

Code information

LOT NUMBER 11798-37631

Distribution pattern

Worldwide Distribution - US including California and the countries of Australia, United Kingdom and Taiwan.

device · product 2 of 4

07-150-10 MIZUHO, DOPPLER PROBE, SLIM, BX 4, REF 138660 The Doppler probe is intended for the intraoperative and transcutaneous evaluation of blood flow.

Z-1999-2014

Recall number: Z-1999-2014
Initiated: May 28, 2014
Classification: Class II
Status: Terminated
Recalling firm: Vascular Technology, Inc.
Quantity: 147

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

Report of the product penetrating the sterile barrier; this could render the product unsterile.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Report of the product penetrating the sterile barrier; this could render the product unsterile.

Code information

LOT NUMBER 11802-37667

Distribution pattern

Worldwide Distribution - US including California and the countries of Australia, United Kingdom and Taiwan.

device · product 3 of 4

07-150-12 MIZUHO, MINI, SLIM, STERILE, BOX OF 4, REF 138665 The Doppler probe is intended for the intraoperative and transcutaneous evaluation of blood flow.

Z-2000-2014

Recall number: Z-2000-2014
Initiated: May 28, 2014
Classification: Class II
Status: Terminated
Recalling firm: Vascular Technology, Inc.
Quantity: 34

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

Report of the product penetrating the sterile barrier; this could render the product unsterile.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Report of the product penetrating the sterile barrier; this could render the product unsterile.

Code information

LOT NUMBER 1516-37698

Distribution pattern

Worldwide Distribution - US including California and the countries of Australia, United Kingdom and Taiwan.

device · product 4 of 4

VTI BAYONET DOPPLER, 20MHz DOPPLER PROBE, SLIM, BX 4, REF 108660 The Doppler probe is intended for the intraoperative and transcutaneous evaluation of blood flow.

Z-2001-2014

Recall number: Z-2001-2014
Initiated: May 28, 2014
Classification: Class II
Status: Terminated
Recalling firm: Vascular Technology, Inc.
Quantity: 25

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

Report of the product penetrating the sterile barrier; this could render the product unsterile.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Report of the product penetrating the sterile barrier; this could render the product unsterile.

Code information

LOT NUMBER 11786-37683

Distribution pattern

Worldwide Distribution - US including California and the countries of Australia, United Kingdom and Taiwan.