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

Recall Z-2537-2020 — VistaSolution, physiological signal transmitter. A software graphical user interface for use by healthcare professionals to display physiological data collected by the wireless remote monitoring system in healthcare settings. This is a secondary, adjunct patient monitor and is not intended to repl

U.S. FDA — Device Enforcement · United States · 2020-05-21 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2537-2020
Date of alert
2020-05-21
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Vitalconnect Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00850490007139
Reported risk: A healthcare provider (HCP) noticed a patient had a lowered historic SpO2 reading that the software should have triggered a notification to the care team, but no notification was found. A software defect was encountered causing the lack of notification. The defect could result in exposing a patient to potential hypoxia for a short window of time. The firm is correcting the software to bring the performance back into compliance with specifications.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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