Devon 31140257Recalls & reported problems
Cardinal Health, Inc. · Light Glove · Class 2
Data updated Oct 18, 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 30884527011739), received between Dec 15, 2016 and Dec 15, 2016 — classified as 1 malfunction.
The most frequently reported specific device problem is “Torn Material” (1 report).
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
- Torn Material1
Patient problems
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 15, 2016Torn Material
IT WAS REPORTED TO COVIDIEN ON (B)(6) 2016 THAT A CUSTOMER HAD AN ISSUE WITH A LITE GLOVE. THE CUSTOMER REPORTS THE LIGHT GLOVES ARE TEARING UP THE MIDDLE UPON APPLICATION TO THE DEVON LIGHT HANDLES. THE MATERIAL SEEMS TO DIFFER IN THICKNESS AND DENSITY DEPENDING ON WHAT SECTION. THE SECTION THAT SLIPS ONTO THE HANDLES IS WHERE THE DAMAGE IS OCCURRING AND APPEARS TO BE MORE TRANSPARENT/THINNER THAN THE CUFF AND TIP.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 6174784 ↗
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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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