MEDLINE MDS6802Recalls & reported problems
Medline Industries, Inc. · GLOVE,EXAM,NTRL,SENSICARE-ICE,W/FILM,MD · Class 1
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00080196555997), received between Jun 1, 2026 and Sep 1, 2026 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Material Split, Cut or Torn” (2 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 Torn2
- Material Puncture/Hole1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
- Exposure to Body Fluids1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 1, 2026Material Puncture/Hole; Material Split, Cut or Torn
Patient problems: Exposure to Body Fluids; No Clinical Signs, Symptoms or Conditions
MAUDE report 50542563 ↗MalfunctionJun 1, 2026Material Split, Cut or Torn
IT WAS REPORTED THAT, MULTIPLE BOXES OF GLOVES ACROSS DIFFERENT SIZES ARE RIPPING BEFORE AND DURING USE. STAFF SOMETIMES NEED TO GO THROUGH MORE THAN 5 GLOVES BEFORE FINDING ONE THAT DOESN'T RIP.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25352755 ↗
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.