KIMTECH 50602Recalls & reported problems
Ansell Healthcare Product · KIMTECH PURPLE NITRILE-XTRA (S) POWDER-FREE EXAM GLOVES · Class 1
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10076490711426), received between Nov 24, 2025 and Nov 24, 2025 — classified as 1 injury.
The most frequently reported specific device problem is “Component Incompatible” (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
- Component Incompatible1
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.
InjuryNov 24, 2025Component Incompatible; Component Incompatible
2 INCIDENTS HAVE RECENTLY REPORTED ADVERSE REACTIONS ASSOCIATED WITH GLOVE USE. THEY NOTED INCREASED INCIDENCE OF GLOVE TEARING IN THE PALM AREA, EXCESSIVE FLUID RETENTION INSIDE THE GLOVES, AND A NOTICEABLE REDUCTION IN GLOVE MATERIAL THICKNESS, RESULTING IN ACCELERATED LIQUID PENETRATION. THE ONLY SUBSTANCES USED IN CONJUNCTION WITH THE GLOVES, ASIDE FROM MUNICIPAL (CITY) WATER AND VE WATER, INCLUDE AN ENZYMATIC CLEANER SUPPLIED BY (B)(4). ONE EMPLOYEE SOUGHT EVALUATION FROM BOTH THE COMPANY PHYSICIAN AND AN OUTSIDE DERMATOLOGIST AND WAS PRESCRIBED A CORTICOSTEROID CREAM, WHICH PROVIDED SYMPTOM RELIEF. THIS EMPLOYEE IS CURRENTLY UNDERGOING MEDICAL TREATMENT. ADDITIONALLY, FOLLOWING CONSULTATION WITH THE COMPANY PHYSICIAN, SUPPLEMENTARY SKIN CARE PRODUCTS WERE PROVIDED FOR THIS INDIVIDUAL.
Patient problems: Local Reaction
MAUDE report 23633470 ↗
Other Polymer Patient Examination Glove devices
- Good Works 72-50602Bosma Enterprises · Polymer Patient Examination Glove1 recall0 reports
- 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 and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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