MEDLINE FG3003Recalls & reported problems
Medline Industries, Inc. · GLOVE,EXAM,NITRILE,FG TOUCH, 300, L · Class 1
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 00888277362751), received between Jul 10, 2026 and Sep 29, 2026 — classified as 5 malfunctions.
The most frequently reported specific device problem is “Material Split, Cut or Torn” (5 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 Torn5
Patient problems
- No Clinical Signs, Symptoms or Conditions5
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 29, 2026Material Split, Cut or Torn
It was reported that every time the DPM attempted to put the glove on it tore. He said the glove felt sticky inside as well.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50931845 ↗MalfunctionSep 24, 2026Material Split, Cut or Torn
It was reported that "The large size gloves that we have are of extremely poor quality. many are torn while still in the box. I am having at least 3-4 torn gloves daily".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50883987 ↗MalfunctionSep 8, 2026Material Split, Cut or Torn
It was reported that "These gloves rip easily while putting them on."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50667090 ↗MalfunctionAug 12, 2026Material Split, Cut or Torn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50225801 ↗MalfunctionJul 10, 2026Material Split, Cut or Torn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25788022 ↗
Other Polymer patient examination glove devices
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- Halyard 47461O&M Halyard, Inc. · Polymer patient examination glove1 recall0 reports
- Bosma Enterprises 72-50903Bosma Enterprises · Polymer Patient Examination Glove1 recall0 reports
- Bosma Enterprises 72-50902Bosma Enterprises · Polymer Patient Examination Glove1 recall0 reports
- 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.