NATUS NEUROLOGY XVLB04Recalls & reported problems
Natus Neurology Incorporated · VERSALAB APM TWIN · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00382830027885), received between Dec 23, 2019 and Dec 23, 2019 — classified as 1 malfunction.
The most frequently reported specific device problem is “Device Sensing Problem” (1 report).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Most reported problems
Device problems
- Device Sensing Problem1
- Environmental Compatibility Problem1
Patient problems
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 23, 2019Device Sensing Problem; Environmental Compatibility Problem; Device Sensing Problem; Environmental Compatibility Problem
USER UNABLE TO HEAR FETAL HEARTBEAT.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 9512905 ↗
Other System, Monitoring, Perinatal devices
- Avalon Fetal Monitor FM30 Avalon FM30 Fetal MonitorPhilips Medizin Systeme Böblingen GmbH · SYSTEM, MONITORING, PERINATAL1 recall11 deaths142 reports
- Avalon Fetal Monitor FM20 Avalon FM20 Fetal MonitorPhilips Medizin Systeme Böblingen GmbH · SYSTEM, MONITORING, PERINATAL1 recall126 reports
- Avalon Ultrasound TransducerPhilips Medizin Systeme Böblingen GmbH · System, Monitoring, Perinatal1 recall2 deaths41 reports
- Avalon Fetal Monitor FM50 Avalon FM50 Fetal MonitorPhilips Medizin Systeme Böblingen GmbH · SYSTEM, MONITORING, PERINATAL9 deaths51 reports
- Central Monitoring System MFM-CNS LiteEdan Instruments, Inc. · System, Monitoring, Perinatal1 recall0 reports
- Fetal & maternal monitor F6 ExpressEdan Instruments, Inc. · System, Monitoring, Perinatal1 recall0 reports
- Fetal & maternal monitor F9Edan Instruments, Inc. · System, Monitoring, Perinatal1 recall0 reports
- Central Monitoring System MFM-CNSEdan Instruments, Inc. · System, Monitoring, Perinatal1 recall0 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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