Integra® Duo 90622Recalls & reported problems
Integra Lifesciences (Ireland) Limited · Integra® Duo Duo Lithium Ion Batteries - Quantity Two · Class 2
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10381780490708), received between Feb 10, 2025 and Feb 10, 2025 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Battery Problem” (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.
Reports received per month
Most reported problems
Device problems
- Battery Problem2
- Premature Discharge of Battery2
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 10, 2025Premature Discharge of Battery; Battery Problem; Premature Discharge of Battery; Battery Problem
MalfunctionFeb 10, 2025Premature Discharge of Battery; Battery Problem; Premature Discharge of Battery; Battery Problem
Other Light, headband, surgical devices
- Integra® Duo 90620USIntegra Lifesciences (Ireland) Limited · Light, headband, surgical33 reports
- Integra® Duo 90600Integra Lifesciences (Ireland) Limited · Light, headband, surgical10 reports
- Welch Allyn, Inc. 901067Welch Allyn, Inc. · Light, headband, surgical1 report
- Integra® 90520USIntegra Lifesciences Production Corporation · Light, headband, surgical1 report
- Welch Allyn, Inc. 901069Welch Allyn, Inc. · Light, headband, surgical1 report
- Integra® 90500Integra Lifesciences Production Corporation · Light, headband, surgical1 report
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.