Facility

VASCULAR TECHNOLOGY INCORPORATED

2 recall(s) on record — most severe on record: Class II.

Key facts

2recalls · worst Class II

1inspections · worst NAI

—warning letters in our data

Recalls are listed for the parent company: openFDA recall records do not name a facility. How we attribute records

FDA Establishment Identifier (FEI)	1221072
Establishment type	Manufacture Medical Device
Location	12 MURPHY DR. NASHUA, NH, US 03062
Registration status	Active · expires 2026
Parent company	VASCULAR TECHNOLOGY INCORPORATED (owner-operator 1221072)
Brand names	VTI 20 MHz Disposable Doppler Probe Bayonet Style Slim Handle, Box; VTI Power Cord: Hospital Europe; Mizuho 07-150-07 Disposable Doppler Probe for Neurosurgery, Box; GEM IntraOp Doppler, Hand-Held Dopplers; VTI 8 MHz Surgical Doppler Transceiver, AC; Mizuho Power Supply Desktop 90-264 VAC; Edwards FLO-003S Ultrasonic Blood Flow Detector Straight Probe, Box; Mizuho 07-150-12 20 MHz Micro Disposable Doppler Probe, Box; VTI Power Cord: Hospital United Kingdom; VTI Power Cord: Hospital US; 8 MHz Kelly Endonasal Disposable Doppler Probe, Box; FLO-001 FLOtector Ultrasonic Blood Flow Detector

Activity by year

Recalls (2)
Inspections (1)

Devices registered here (1)

Flowmeter, Blood, Cardiovascular
Product code DPW (opens in a new tab) · Class II · Cardiovascular · 21 CFR 870.2100

Recalls & enforcement

Class IITerminated2018-06-19
Device maybe mislabeled as a 20 MHz Doppler transceiver instead of an 8 MHz Doppler transceiver
Class IITerminated2014-05-28
Report of the product penetrating the sterile barrier; this could render the product unsterile.

FDA inspections (1)

NAI2016-08-03
No Action Indicated · Compliance: Devices

Source: U.S. FDA Inspections Dashboard (opens in a new tab) (device inspection classifications, 2016–present). Data as of 2026-10-06. The dashboard profile can take several seconds to load.

All facilities operated by VASCULAR TECHNOLOGY INCORPORATED

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)

Cite this record

RegWarden. “VASCULAR TECHNOLOGY INCORPORATED (FEI 1221072) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/1221072-vascular-technology-incorporated/

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