Moberg recalls CNS-350 neuromonitoring devices with battery leakage that may cause skin corrosion. Affected units have specific serial numbers; stop using immediately to avoid injury.
Battery leakage can cause corrosion to the metal enclosure near the electrical interface. Prolonged contact to corrosive materials could cause injury to skin. DOC
Moberg recalls its CNS-350 neuromonitoring devices due to battery leakage that can cause skin corrosion. This poses a risk of injury from prolonged contact with corrosive materials, so affected users should stop using the device immediately.
The battery in the CNS-350 device can leak corrosive materials that may cause skin irritation or injury with prolonged contact. This risk is higher when the device is handled frequently or left in contact with skin for extended periods.
Medical professionals using the CNS-350 neuromonitoring system for short-term neurological monitoring are most at risk. Patients or caregivers handling the device could also be affected if battery leakage occurs.
Check for serial numbers starting with A-CNS-22502 to A-CNS-22591. The device is a short-term neurological monitoring system that collects and displays physiological measurements.
The battery leakage can cause skin corrosion, so immediately stop using the CNS-350 device if you have the affected serial numbers.
The recalled device is the Moberg CNS-350 neuromonitoring system with serial numbers from A-CNS-22502 to A-CNS-22591.
Check if your device has a serial number starting with A-CNS-22502 to A-CNS-22591. The CNS-350 is a short-term neurological monitoring system.
The recall does not mention a fix or remedy; affected users should stop using the device immediately.
We’ve drafted a message you can send Moberg to request your refund or repair — edit it as you like.
Subject: Recall Z-1338-2023 — Moberg Moberg Hello, I own a Moberg that is covered by recall Z-1338-2023 from Moberg. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
