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MEDLINE FG3002Recalls & reported problems

Medline Industries, Inc. · GLOVE,EXAM,NITRILE,FG TOUCH, 300, M · Class 1

Adverse event reports
21
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 21 adverse event reports that list this exact device (DI 00888277362744), received between May 17, 2026 and Sep 30, 2026 — classified as 21 malfunctions.

The most frequently reported specific device problem is “Material Split, Cut or Torn” (19 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

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 5 reportsJun 2026: 1 reportsJul 2026: 5 reportsAug 2026: 3 reportsSep 2026: 7 reportsOct 2026: 0 reports2024202520267
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Material Split, Cut or Torn19
  • Fluid/Blood Leak1
  • Nonstandard Device1
  • Packaging Problem1
  • Tear, Rip or Hole in Device Packaging1

Patient problems

  • No Clinical Signs, Symptoms or Conditions21

Recent adverse event reports

The 21 most recent of 21 reports, in the reporter's own words as published by the FDA.

  • MalfunctionSep 30, 2026Material Split, Cut or Torn

    It was reported that "gloves are tearing too easily or at least easier than they were before" and "customer beleives the mil might be different than the older gloves."

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50946710 ↗
  • MalfunctionSep 18, 2026Material Split, Cut or Torn

    It was reported that "some reason the thumbs are destroyed in the gloves and we couldn't use half the box."

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50819437 ↗
  • MalfunctionSep 14, 2026Material Split, Cut or Torn

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50763265 ↗
  • MalfunctionSep 10, 2026Material Split, Cut or Torn

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50722903 ↗
  • MalfunctionSep 2, 2026Nonstandard Device; Material Split, Cut or Torn

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50567829 ↗
  • MalfunctionSep 2, 2026Packaging Problem

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50564628 ↗
  • MalfunctionSep 1, 2026Material Split, Cut or Torn

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50551506 ↗
  • MalfunctionAug 31, 2026Fluid/Blood Leak; Material Split, Cut or Torn

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50523570 ↗
  • MalfunctionAug 24, 2026Material Split, Cut or Torn

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50419454 ↗
  • MalfunctionAug 6, 2026Tear, Rip or Hole in Device Packaging

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50163847 ↗
  • MalfunctionJul 20, 2026Material Split, Cut or Torn

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 25879033 ↗
  • MalfunctionJul 14, 2026Material Split, Cut or Torn

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 25821475 ↗
  • MalfunctionJul 10, 2026Material Split, Cut or Torn

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 25788024 ↗
  • MalfunctionJul 8, 2026Material Split, Cut or Torn

    IT WAS REPORTED BY THE CUSTOMER THAT ONE OF THE BOXES OF GLOVES RECEIVED ARE FULL OF HOLES (MANY OF THEM) OR ARE RIPPED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 25752834 ↗
  • MalfunctionJul 2, 2026Material Split, Cut or Torn

    IT WAS REPORTED BY THE CUSTOMER THAT THE GLOVES ARE LOW QUALITY, AND THEY RIP EASILY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 25696506 ↗
  • MalfunctionJun 18, 2026Material Split, Cut or Torn

    IT WAS REPORTED "GLOVES RIP WHEN YOU PUT THEM ON."

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 25555425 ↗
  • MalfunctionMay 17, 2026Material Split, Cut or Torn

    IT WAS REPORTED THAT, GLOVES ARE RIPPING EASILY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 25196775 ↗
  • MalfunctionMay 17, 2026Material Split, Cut or Torn

    IT WAS REPORTED THAT, GLOVES RIPPED WHEN DONNED. RIPPED GLOVES DISCARDED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 25196510 ↗
  • MalfunctionMay 17, 2026Material Split, Cut or Torn

    IT WAS REPORTED THAT, GLOVES RIPPED WHEN THE NURSE DONNING FOR PPE. RIPPED GLOVES DISCARDED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 25196509 ↗
  • MalfunctionMay 17, 2026Material Split, Cut or Torn

    IT WAS REPORTED THAT, THE GLOVES RIP EASILY UPON DONNING.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 25196505 ↗
  • MalfunctionMay 17, 2026Material Split, Cut or Torn

    IT WAS REPORTED THAT, GLOVES RIP UPON DONNING. RIPPED GLOVES DISCARDED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 25196504 ↗

Other Polymer patient examination glove devices

All Polymer patient examination glove devices →

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