Mizuho 07-150-10 Disposable Doppler Probe for Neurosurgery, Box 138660Recalls & reported problems
Vascular Technology, Incorporated · Part Number 138660, Mizuho 07-150-10 Disposable Doppler Probe for Neurosurgery, Box · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10817122020208), received between Aug 10, 2020 and Aug 10, 2020 — classified as 1 injury.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (1 report).
4 other recalls cover devices cleared under the same FDA submission (K082870); they may or may not involve this specific model.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Most reported problems
Device problems
- Insufficient Device Problem Information1
Patient problems
- Aneurysm1
- Patient Problem/Medical Problem1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryAug 10, 2020Insufficient Device Problem Information; Insufficient Device Problem Information
THE HOSPITAL REPRESENTATIVE, MR (B)(6) STATES, "THERE WS AN ACCIDENTAL VASCULAR INJURY IN AN ANEURYSM SURGERY WITH THE CURRENT MICRO DOPPLER PROBES, WHICH ARE NO LONGER COMPLETELY ENCASED IN A ROUND-ENDED ATRAUMATIC PLASTIC SHEATH, INCLUDING THE PROBE TIP, BUT ARE ENCASED IN A RELATIVELY SHARP-EDGED, CYLINDRICAL-ENDED PLASTIC SHEATH". ADDITION INFROMATION PROVIDED ON 03-AUG-2020 - THE INJURED VESSEL WAS COAGULATED". SO INJURY OCCURED BUT COAGULATED AND PATIENT IS FINE.
Patient problems: Aneurysm; Patient Problem/Medical Problem
MAUDE report 10384823 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K082870. One submission often covers many models, so check the product and lot details in each record.
- Z-1999-2014 · May 28, 2014 · Terminated07-150-10 MIZUHO, DOPPLER PROBE, SLIM, BX 4, REF 138660 The Doppler probe is intended for the intraoperative and transcutaneous evaluation of blood flow.
- Z-2001-2014 · May 28, 2014 · TerminatedVTI 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-1998-2014 · May 28, 2014 · Terminated07-150-07 MIZUHO, MAL DISP DOPPLER PROBE BX 4, REF 138200 The Doppler probe is intended for the intraoperative and transcutaneous evaluation of blood flow.
- Z-2000-2014 · May 28, 2014 · Terminated07-150-12 MIZUHO, MINI, SLIM, STERILE, BOX OF 4, REF 138665 The Doppler probe is intended for the intraoperative and transcutaneous evaluation of blood flow.
Other FLOWMETER, BLOOD, CARDIOVASCULAR devices
- GEM FLOW COUPLER MONITOR GEM1020M-2Synovis Micro Companies Alliance, Inc · FLOWMETER, BLOOD, CARDIOVASCULAR2 recalls0 reports
- Dual Adhesive Strap FP120-FOT01-0051929803 Ontario Corp · Flowmeter, Blood, Cardiovascular1 recall0 reports
- BiDop 3Koven Technology, Inc. · Flowmeter, Blood, Cardiovascular1 recall0 reports
- GEM FLOW COUPLER GEM2752 FCSynovis Micro Companies Alliance, Inc · FLOWMETER, BLOOD, CARDIOVASCULAR4 reports
- GEM FLOW COUPLER GEM2753 FCSynovis Micro Companies Alliance, Inc · FLOWMETER, BLOOD, CARDIOVASCULAR4 reports
- GEM FLOW COUPLER GEM2755 FCSynovis Micro Companies Alliance, Inc · FLOWMETER, BLOOD, CARDIOVASCULAR1 report
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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