Medline Industries, Inc. PAIN1808Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10195327145446), received between Mar 17, 2023 and Sep 25, 2026 — classified as 1 injury, 2 malfunctions.

The most frequently reported specific device problem is “Obstruction of Flow” (2 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 18, 2026.

Most reported problems

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 25, 2026Obstruction of Flow

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50904097 ↗
• MalfunctionSep 21, 2026Obstruction of Flow

  It was reported that "3 reports of epidural catheters being occluded, including at least one from the CSE kit with lot information."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50838161 ↗
• InjuryMar 17, 2023Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  ACCORDING TO THE FACILITY AN EPIDURAL CATHETER WAS INITIALLY PLACED WITHOUT COMPLICATIONS. PER THE FACILITY AFTER ASSESSING THE CATHETER, LOCAL ANESTHETIC WAS NOT ADMINISTERED DUE TO HIGH-RESISTANCE IN THE CATHETER.

  Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available

  MAUDE report 16564610 ↗