CAMINO® 110-4LRecalls & reported problems
Integra Lifesciences Corporation · CAMINO® INTRACRANIAL PRESSURE MONITORING CATHETER WITH LICOX BOLT FITTING · Class 2
All models of CAMINO (6)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10381780023661), received between Apr 19, 2019 and Nov 26, 2019 — classified as 1 injury, 2 malfunctions.
The most frequently reported specific device problem is “Incorrect, Inadequate or Imprecise Result or Readings” (2 reports).
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
- Incorrect, Inadequate or Imprecise Result or Readings2
- Low Test Results1
Patient problems
- No Known Impact Or Consequence To Patient3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryNov 26, 2019Low Test Results; Low Test Results
LICOX ICP METER WAS INSERTED TO PATIENT FOR TWO DAYS WITH A READING OF 2, HOWEVER PATIENT GOT WORSE. WHEN UNIT REPLACED WITH ANOTHER, READING WAS 32.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 9376128 ↗MalfunctionAug 14, 2019Incorrect, Inadequate or Imprecise Result or Readings; Incorrect, Inadequate or Imprecise Result or Readings
CATHETER GAVE DIFFERENT WAVEFORM READINGS AFTER IMPLANTATION.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8894061 ↗MalfunctionApr 19, 2019Incorrect, Inadequate or Imprecise Result or Readings; Incorrect, Inadequate or Imprecise Result or Readings
CATHETER FAILED AFTER INSTALLATION, REQUIRING A NEW ONE.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8533472 ↗
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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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