CAMINO® 110-4HM (REF 1104HM)Recalls & reported problems
Natus Medical Incorporated · MICRO VENTRICULAR BOLT PRESSURE MONITORING KIT · Class 2
Data updated Oct 16, 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 00382830047524), received between Jul 31, 2024 and Jul 31, 2024 — classified as 1 malfunction.
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 16, 2026.
Reports received per month
Most reported problems
Patient problems
- Vessel Or Plaque, Device Embedded In1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 31, 2024
DURING PLACEMENT OF AN INTERCRANIAL PRESSURE MONITORING BOLT THE NEUROSURGEON NOTED THAT THE BOLT WOULD NOT SCREW INTO THE HOLE MADE BY THE DRILL. WHILE REPOSITIONING IT, THE BOLT BROKE OFF INSIDE THE PATIENT'S HEAD. THE NEUROSURGEON WAS ABLE TO RETRIEVE THE PIECE REMAINING IN THE PATIENT WITH A CLAMP. THE NEUROSURGEON WAS THEN ABLE TO PLACE A VENTRICULOSTOMY.
Patient problems: Vessel Or Plaque, Device Embedded In
MAUDE report 19885316 ↗
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- CereLink™ 826851Integra Lifesciences Production Corporation · Device, monitoring, intracranial pressure96 reports
- Becker® 26040Medtronic Ps Medical, Inc. · Device, monitoring, intracranial pressure1 recall46 reports
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- Codman Microsensor® 826631Integra Lifesciences Production Corporation · Device, monitoring, intracranial pressure75 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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