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ESTEEM S88RX02Recalls & reported problems

Cardinal Health 200, LLC · Synthetic with Neu-Thera® Powder-Free Vinyl Exam Gloves Stretchy Protects Restores Moisturizes · Class 1

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 20885380135405), received between Apr 7, 2017 and Apr 7, 2017 — classified as 1 injury.

The most frequently reported specific device problem is “Patient-Device Incompatibility” (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.

Most reported problems

Device problems

  • Patient-Device Incompatibility1

Patient problems

  • Rash1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryApr 7, 2017Patient-Device Incompatibility

    BASED ON INFORMATION RECEIVED FROM THE CUSTOMER AN EMPLOYEE WAS WEARING GLOVES S88RX02. THE EMPLOYEE THEN BROKE OUT IN HIVES. THE EMPLOYEE WENT TO EMPLOYEE HEALTH AND WAS PROVIDED BENADRYL. THIS WAS THE FIRST TIME THE EMPLOYEE WORE THESE GLOVES.  SHE IS DOING FINE NOW.

    Patient problems: Rash

    MAUDE report 6471591 ↗

Other Vinyl patient examination glove devices

All Vinyl patient examination glove devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.