Medline MG5002Recalls & reported problems
Medline Industries, Inc. · GLOVE, EXAM, NITRILE, PF, W/ FILM, M · Class 1
- Adverse event reports
- 7
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 00197344024936), received between Jun 30, 2026 and Sep 2, 2026 — classified as 7 malfunctions.
The most frequently reported specific device problem is “Material Split, Cut or Torn” (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, 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
- Material Split, Cut or Torn7
Patient problems
- No Clinical Signs, Symptoms or Conditions7
Recent adverse event reports
The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 2, 2026Material Split, Cut or Torn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50570506 ↗MalfunctionSep 1, 2026Material Split, Cut or Torn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50551558 ↗MalfunctionAug 31, 2026Material Split, Cut or Torn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50521682 ↗MalfunctionAug 31, 2026Material Split, Cut or Torn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50520527 ↗MalfunctionJul 22, 2026Material Split, Cut or Torn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25904448 ↗MalfunctionJun 30, 2026Material Split, Cut or Torn
IT WAS REPORTED BY THE CUSTOMER THAT WHEN PULLING OUT GLOVES, MANY ARE COMING OUT AND THEN WHEN TRYING TO PULL THEM APART, THEY ARE RIPPING.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25669704 ↗MalfunctionJun 30, 2026Material Split, Cut or Torn
IT WAS REPORTED BY THE CUSTOMER THAT WHEN PULLING OUT GLOVES, MANY ARE COMING OUT AND THEN WHEN TRYING TO PULL THEM APART, THEY ARE RIPPING.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25669702 ↗
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- Halyard 48773O&M Halyard, Inc. · Polymer patient examination glove1 recall0 reports
- Bosma Enterprises 72-50803Bosma Enterprises · Polymer Patient Examination Glove1 recall0 reports
- Halyard 47460O&M Halyard, Inc. · Polymer patient examination glove1 recall0 reports
- Bosma Enterprises 72-50900Bosma Enterprises · Polymer Patient Examination Glove1 recall0 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.