Medline OR510TRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10888277319134), received between Sep 15, 2026 and Sep 28, 2026 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Misconnection” (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. How this data works · Data updated Oct 13, 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 28, 2026Obstruction of Flow; Suction Failure

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50926589 ↗
• MalfunctionSep 15, 2026Misconnection

  It was reported that "The tubing is not staying connected to the machine."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50773178 ↗