Matrx E2 Standard Back E2SRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07540147000424), received between Jun 6, 2025 and Jun 6, 2025 — classified as 1 injury.

The most frequently reported specific device problem is “Deformation Due to Compressive Stress” (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.

• InjuryJun 6, 2025Deformation Due to Compressive Stress; Deformation Due to Compressive Stress

  ON (B)(6) 2025, MEDBLOC (THE DISTRIBUTOR) NOTIFIED MOTION CONCEPTS LP OF AN INCIDENT INVOLVING A MATRX BACKREST INSTALLED ON A MOTION CONCEPTS WHEELCHAIR. ACCORDING TO THE NOTIFICATION, THE SYSTEM HAD BEEN SOLD TO NATIONAL SEATING & MOBILITY - PHOENIX, AZ, WHO IS ALSO RESPONSIBLE FOR ITS ONGOING MAINTENANCE. THE END-USER REPORTED TO THE DEALER THAT THE RIGHT-HAND SIDE OF THE MATRX BACKREST LACKED THE SAME LEVEL OF CUSHIONING AS THE LEFT SIDE. THIS ASYMMETRY WAS REPORTED AS THE CAUSE OF A STAGE 2 PRESSURE SORE ON USER'S RIGHT SIDE, NEAR THE RIB AREA. IT WAS ALSO NOTED THAT THE END-USER HAS A C5-C6 COMPLETE QUADRIPLEGIA DIAGNOSIS AND TYPICALLY USES THE WHEELCHAIR FOR APPROXIMATELY 3 TO 4 HOURS PER DAY.

  Patient problems: Pressure Sore/Ulcer

  MAUDE report 22159542 ↗