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Halyard 55082Recalls & reported problems

O&M Halyard, Inc. · HALYARD* PURPLE NITRILE* Exam Glove Medium · Class 1

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 20680651550822), received between Oct 3, 2017 and Oct 3, 2017 — classified as 1 injury.

The most frequently reported specific device problem is “Protective Measures Problem” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Protective Measures Problem1

Patient problems

  • Burn(s)1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryOct 3, 2017Protective Measures Problem; Protective Measures Problem

    IT WAS REPORTED THAT A CUSTOMER WAS POURING BOILING NITRIC ACID INTO A BEAKER AND WITHOUT WARNING A CHEMICAL REACTION OCCURRED CAUSING ACID TO SPILL ONTO THE WRIST. THE BOILING ACID BURNED THROUGH THE PURPLE NITRILE GLOVES CAUSING THIRD-DEGREE BURNS, WHICH REQUIRED A SKIN GRAFT USING SKIN FROM THE CUSTOMER¿S RIGHT LEG. NO ADDITIONAL INFORMATION WAS PROVIDED.

    Patient problems: Burn(s)

    MAUDE report 6912413 ↗

Other Patient examination glove, specialty devices

All Patient examination glove, specialty devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.