Drug recall
Moberg Component Neuromonitoring System (CNS Monitor)-Intended as a short-term neurological monitoring system…
FDA recall event 91782 · Class II · Moberg Research, Inc.
Key facts
| Event ID | 91782 |
|---|---|
| Recall numbers | Z-1338-2023 |
| Recalling firm | Moberg Research, Inc. |
| Product type | Devices |
| Products | 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 |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Battery leakage can cause corrosion to the metal enclosure near the electrical interface. Prolonged contact to corrosive materials could cause injury to skin. DOC |
| Initiation date | Feb 20, 2023 |
| Report date | Apr 12, 2023 |
| City | Ambler |
| State | PA |
| Country | United States |
| FEI number | 3007880955 |
At a glance
- 1–9 Products in this recall
- None FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: