Medline FG100SRecalls & reported problems
Medline Industries, Inc. · FG TOUCH NITRILE EXAM GLOVES, 100CT, SM · Class 1
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00888277653941), received between May 17, 2026 and Sep 2, 2026 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Material Split, Cut or Torn” (3 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 Torn3
- Material Integrity Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions4
Recent adverse event reports
The 4 most recent of 4 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 50573039 ↗MalfunctionJul 31, 2026Material Split, Cut or Torn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50104328 ↗MalfunctionMay 20, 2026Material Integrity Problem
IT WAS REPORTED THAT WHILE WEARING GLOVES VASELINE AND BETADINE WERE ABLE TO SOAK THROUGH THE GLOVES STAINING HANDS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25231946 ↗MalfunctionMay 17, 2026Material Split, Cut or Torn
IT WAS REPORTED THAT, GLOVES WERE RIPPED ALONG THE SIDE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25196778 ↗
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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
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- 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.