MEDLINE KX248V21ERecalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00193489179937), received between May 7, 2026 and Sep 28, 2026 — classified as 4 malfunctions.

The most frequently reported specific device problem is “Material Split, Cut or Torn” (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 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 28, 2026Material Split, Cut or Torn

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50924879 ↗
• MalfunctionMay 7, 2026No Apparent Adverse Event

  CUSTOMER STATED "THE BRAKES ON THE WHEELCHAIR ARE MISSING".

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25113968 ↗
• MalfunctionMay 7, 2026No Apparent Adverse Event

  CUSTOMER STATED "THE RUBBER CAME OFF THE REAR WHEEL, AND IT BENT THE WHEEL".

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25113967 ↗
• MalfunctionMay 7, 2026No Apparent Adverse Event

  CUSTOMER STATED "THE WHEELCHAIR HAS NO BRAKES".

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25113966 ↗