Medline PRO31760Recalls & reported problems
Medline Industries, Inc. · GLOVE,EXAM,CHEMO,NITRILE,ALOE,PF,TXT,XS · 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 00884389965378), received between Sep 14, 2026 and Sep 14, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Biocompatibility” (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
- Biocompatibility1
Patient problems
- Local Reaction1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 14, 2026Biocompatibility
It was reported that "CST INSISTS THAT THESE GLOVES ARE NOT NITRILE GLOVES AND THEY ARE IN FACT LATEX GLOVES" and "SHE STATES THAT SEVERAL DOCTORS, NURSES, AND OTHER PERSONNEL'S HANDS ARE SWELLING AND HAVING AN ALERGIC REACTION."
Patient problems: Local Reaction
MAUDE report 50754428 ↗
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.