Medline Industries, Inc. PHS988149DRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10195327601430), received between Aug 12, 2026 and Aug 12, 2026 — classified as 1 malfunction.

The most frequently reported specific device problem is “Material Frayed” (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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Recent adverse event reports

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

• MalfunctionAug 12, 2026Material Frayed

  It was reported that "the blue towels in the vaginal delivery packs are leaving lint on the patient and provider gloves" and "The concern is that lint is being left behind in the vagina."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50220214 ↗