Ambler, PA, United States
Moberg Research, Inc. recalls
1 recall recorded since 2018, most recently on 20 February 2023. 1 is listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)1
Terminated or completed0
Class I (FDA)0
Ongoing Class II Medical devices
- Recall started
- 20 February 2023
- Reason
- Battery leakage can cause corrosion to the metal enclosure near the electrical interface. Prolonged contact to corrosive materials could cause injury to skin. DOC
- Distribution
- Worldwide distribution - US Nationwide and the countries of France, Germany, Italy, Sweden.
- Initiated
- Voluntary: Firm initiated
- Recall number
- 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
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.