Medline OR56ARecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10888277319172), received between Aug 12, 2026 and Sep 8, 2026 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Suction Problem” (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. 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 8, 2026Suction Problem; Fitting Problem

  It was reported that some of the tubing does not fit correctly and is unable to create the suction needed.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50668269 ↗
• MalfunctionAug 12, 2026Suction Problem

  It was reported that Pt was oral suctioning with Yankeur and the set up stop working. Noted Medline Suction tubing Ref (b)(4) when connected to the cannister, the suction stopped. Used another suction tubing to a new cannister and same thing happened, the suction stopped. Another Argyle suction tubing was used and no issues reported.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50222326 ↗