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CAMINORecalls & reported problems across all models

Integra Lifesciences Corporation · 6 models in the FDA device registry

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
32
Deaths reported
0
Injuries reported
4
Recalls
0

We found 6 models of CAMINO by Integra Lifesciences Corporation in the FDA's device registry (GUDID). Together they are named in 32 adverse event reports in the FDA's MAUDE database, received between Nov 16, 2017 and May 26, 2021 — classified as 4 injuries, 28 malfunctions.

The most frequently reported specific device problem is “Output Problem” (7 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. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works

Most reported CAMINO problems

Device problems

  • Output Problem7
  • Unable to Obtain Readings7
  • Incorrect, Inadequate or Imprecise Result or Readings6
  • Device Operational Issue3
  • Device Issue2
  • Device Sensing Problem2
  • Break1
  • Degraded1

Patient problems

  • No Known Impact Or Consequence To Patient28
  • No Consequences Or Impact To Patient5
  • Foreign Body In Patient1
  • No Clinical Signs, Symptoms or Conditions1
  • Test Result1

CAMINO models

6 models, most reported first. Each model has its own page with its reports, recalls and device details.

Recent CAMINO adverse event reports

The 15 most recent reports across all models, in the reporter's own words as published by the FDA.

Other Integra Lifesciences Corporation products

All Integra Lifesciences Corporation devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page