Walgreens 218257Recalls & reported problems

Summary

The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 00311917150970), received between Feb 24, 2021 and Sep 21, 2026 — classified as 1 injury, 4 malfunctions.

The most frequently reported specific device problem is “Material Split, Cut or Torn” (4 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Recent adverse event reports

The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 21, 2026Material Split, Cut or Torn

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50840059 ↗
• MalfunctionSep 10, 2026Material Split, Cut or Torn

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50717168 ↗
• MalfunctionAug 31, 2026Material Split, Cut or Torn

  It was reported that "GLOVES RIPS ON BOTTOM EVERYTIME SHE PUT THEM ON AS WELL RIPS ON FINGERS."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50524930 ↗
• MalfunctionMay 1, 2026Material Split, Cut or Torn

  IT WAS REPORTED THAT THE CUSTOMER CALLED IN TO REPORT PURCHASING A BOX OF GLOVES 2 WEEKS AGO AT WALGREENS, SHE IS AT THE END USE OF THE GLOVES WHEN SHE NOTICES MAJORITY OF THE GLOVES WERE CUT OFF AT THE WRIST.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25061979 ↗
• InjuryFeb 24, 2021Patient-Device Incompatibility

  IT WAS REPORTED THAT THE FIRST TIME THAT THE EMPLOYEE USED THE GLOVES SHE BEGAN TO EXPERIENCE SWELLING ON BOTH OF HER HANDS AND ARMS WITHIN TWENTY MINUTES.

  Patient problems: Hypersensitivity/Allergic reaction

  MAUDE report 11375029 ↗