MEDLINE MDS192076Recalls & reported problems
Medline Industries, Inc. · GLOVE,EXAM,VINYL,SYNTHETIC,PF,LF,LG · Class 1
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00080196167992), received between Jul 27, 2026 and Jul 27, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Material Split, Cut or Torn” (1 report).
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 Torn1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 27, 2026Material Split, Cut or Torn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50019440 ↗
Other Vinyl patient examination glove devices
- Walgreens 218257Walgreen CO. · Vinyl Patient Examination Glove5 reports
- Medline MDS195174Medline Industries, Inc. · Vinyl patient examination glove3 reports
- MEDLINE 4GVINLCMedline Industries, Inc. · Vinyl patient examination glove2 reports
- MEDLINE 4GVINXLCMedline Industries, Inc. · Vinyl patient examination glove2 reports
- MEDLINE MDS1285Medline Industries, Inc. · Vinyl patient examination glove2 reports
- MEDLINE MDS195175Medline Industries, Inc. · Vinyl patient examination glove2 reports
- Walgreens 426041Walgreen CO. · Vinyl Patient Examination Glove1 report
- MEDLINE 484401Medline Industries, Inc. · Vinyl patient examination glove1 report
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.