Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2275-2019 — HS70A Diagnostic Ultrasound System Version 2.01.00, 2.01.01, 2.01.02, 2.01.03, 2.01.04, 2.01.05, 2.01.06, 1.00.06, 1.00.07, 1.00.08, 1.00.09, 1.00.10, 1.00.11, 1.00.12

U.S. FDA — Device Enforcement · United States · 2019-07-25 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2275-2019
Date of alert
2019-07-25
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
NeuroLogica Corporation
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
08806167789220
Reported risk: There is a potential for probes overheating when decreasing the Doppler SV (Sample Volume) size value set by the user in the Doppler Only mode.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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