Medline Industries, Inc. PAIN9010SRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10884389582800), received between Sep 14, 2026 and Sep 21, 2026 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Material Too Soft/Flexible” (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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 21, 2026Packaging Problem

  It was reported that "the sterile barrier for the tray allows betadine to leak through."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50840418 ↗
• MalfunctionSep 14, 2026Material Too Soft/Flexible

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50765418 ↗