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

Recall Z-1338-2023 — Moberg Component Neuromonitoring System (CNS Monitor)-Intended as a short-term neurological monitoring system that collects, displays, and stores multiple physiological measurements Model: CNS-350

U.S. FDA — Device Enforcement · United States · 2023-02-20 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1338-2023
Date of alert
2023-02-20
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Moberg Research, Inc.
Product category
device
Product type
Devices
Reported risk: Battery leakage can cause corrosion to the metal enclosure near the electrical interface. Prolonged contact to corrosive materials could cause injury to skin. DOC
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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