Medline Industries, Inc. PAIN2173Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10198459111761), received between Apr 2, 2025 and Apr 2, 2025 — classified as 1 injury.

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.

• InjuryApr 2, 2025Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  ACCORDING TO THE FACILITY ON 3/3 DURING A C6-7 INTERLAMINAR EPIDURAL STEROID INJECTION, "THE EXTENSION WAS USED TO ADD CONTRAST INTO THE EPIDURAL SPACE. DR. (B)(6) THEN ATTEMPTED TO DISCONNECT THE EXTENSION FROM THE TUOHY NEEDLE PLACED IN THE PATIENT, WHEN HE ATTEMPTED TO DISCONNECT THE EXTENSION WOULD GET "STUCK" IN THE NEEDLE CAUSING THE TUOHY NEEDLE TO SLIGHTLY MOVE CAUSING A SPINAL TAP".

  Patient problems: Low Blood Pressure/ Hypotension

  MAUDE report 21756596 ↗