Centurion CUHG1-INTRecalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 20653160290299), received between Sep 25, 2026 and Sep 30, 2026 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Failure to Power Up” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 30, 2026Failure to Power Up; Failure to Calibrate

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50948163 ↗
• MalfunctionSep 28, 2026Incorrect Measurement

  It was reported that "Impossible to use the device. The numbers indicating the pressure oscillate even though the device is placed flat on the work surface."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50913228 ↗
• MalfunctionSep 25, 2026Incorrect Measurement; Failure to Power Up

  It was reported that a new compartment syndrome kit lit up but remained stuck at an abnormal value of 134 instead of dropping back to 0 before taking the measurement.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50895716 ↗