Medline TRG500SRecalls & reported problems
Medline Industries, Inc. · GLOVE,EXAM,NITRILE,PF,SELECT,SM · Class 1
- Adverse event reports
- 13
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 13 adverse event reports that list this exact device (DI 00888277414214), received between Apr 8, 2026 and Sep 23, 2026 — classified as 13 malfunctions.
The most frequently reported specific device problem is “Material Split, Cut or Torn” (12 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 Torn12
- Material Puncture/Hole1
- Physical Resistance/Sticking1
Patient problems
- No Clinical Signs, Symptoms or Conditions12
- Exposure to Body Fluids1
Recent adverse event reports
The 13 most recent of 13 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 23, 2026Material Split, Cut or Torn
Patient problems: Exposure to Body Fluids
MAUDE report 50870591 ↗MalfunctionSep 11, 2026Material Split, Cut or Torn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50742778 ↗MalfunctionSep 11, 2026Material Split, Cut or Torn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50741744 ↗MalfunctionSep 8, 2026Material Split, Cut or Torn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50676591 ↗MalfunctionSep 7, 2026Material Puncture/Hole
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50651695 ↗MalfunctionSep 7, 2026Material Split, Cut or Torn; Physical Resistance/Sticking
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50650283 ↗MalfunctionJul 29, 2026Material Split, Cut or Torn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50069857 ↗MalfunctionJul 29, 2026Material Split, Cut or Torn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50069856 ↗MalfunctionJul 22, 2026Material Split, Cut or Torn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25907415 ↗MalfunctionJul 8, 2026Material Split, Cut or Torn
IT WAS REPORTED BY THE CUSTOMER THAT GLOVES RIP EASILY WHEN PUTTING ON, OVER 50% TEAR RATE, GLOVES FUSED TOGETHER (PULL 1 AND GET 4 OR 5), GLOVES TEAR WHEN PULLING OUT OF THE BOX.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25752827 ↗MalfunctionJul 3, 2026Material Split, Cut or Torn
IT WAS REPORTED THAT THE NURSING STAFF HAVE NOTICED A DECREASE IN THE QUALITY OF THE BOXES OF GLOVES. GLOVES ARE COMING WITH HOLES, INCOMPLETE GLOVES, AND STACKS ALL WELDED TOGETHER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25708577 ↗MalfunctionMay 29, 2026Material Split, Cut or Torn
IT WAS REPORTED THAT THE GLOVES ARE TORN OUT OF THE BOX.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25338607 ↗MalfunctionApr 8, 2026Material Split, Cut or Torn
ACCORDING TO THE CUSTOMER, THE FINGER ON GLOVE BROKE DURING PATIENT CARE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24817948 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.