Matrx Libra Cushion LCRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07540147000998), received between Mar 6, 2024 and Mar 6, 2024 — classified as 1 injury.

The most frequently reported specific device problem is “Gel Leak” (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 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryMar 6, 2024Gel Leak; Gel Leak

  ON FEBRUARY 13, 2024, MOTION CONCEPTS LP RECEIVED NOTIFICATION FROM MEDBLOC INC. REGARDING AN INCIDENT INVOLVING A MATRX CUSHION. A DEALER IN THE USA (NUMOTION, NASHVILLE, TN) REPORTED AN ISSUE WITH A CUSHION BEING USED BY AN END-USER, ALLEGING A GEL LEAK THAT MAY HAVE LED TO A PRESSURE ULCER ON THE LEFT HIP OF THE USER. CONSEQUENTLY, THE END-USER REQUIRED DEBRIDEMENT, WOUND VAC TREATMENT, AND HOSPITALIZATION. THE ALLEGED LIBRA CUSHION WAS EXCHANGED UNDER WARRANTY; HOWEVER, THE END-USER IS CURRENTLY SEEKING A REPLACEMENT WITH A ROHO CUSHION, FOLLOWING THE RECOMMENDATION OF THE PHYSICAL THERAPIST. ADDITIONALLY, IT WAS NOTED THAT THE END-USER, WHO HAS PARAPLEGIA, TYPICALLY UTILIZES THE WHEELCHAIR FOR APPROXIMATELY 12 HOURS PER DAY. THE DATE OF THE EVENT IS UNKNOWN.

  Patient problems: Ulcer

  MAUDE report 18849774 ↗