MODULAR POWER STANDING SYSTEM MPSSRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00754014711444), received between Mar 12, 2020 and Mar 12, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (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 12, 2020Insufficient Device Problem Information; Insufficient Device Problem Information

  ON 12-FEB-2020, MOTION CONCEPTS WAS NOTIFIED BY MEDBLOC (MOTION CONCEPTS IMPORTER) THAT ONE OF THEIR DEALERS (AFTER THE FALL) WAS NOTIFIED OF AN INCIDENT THAT TOOK PLACE ON (B)(6) 2020. AS PER THE DEALER, THE PATIENT'S WIFE DISCOVERED THAT, THERE WAS AN ABRASION ON THE PATIENT'S BACK AND INFORMED IT TO THEIR FAMILY DOCTOR ON (B)(6) 2020, WHO ENQUIRED WHETHER THERE WAS ANY DAY-TO-DAY CHANGES ON PATIENTS LIFE. THE DOCTOR SUGGESTED THAT THE ABRASION COULD HAVE CAUSED BY A PINCH. AS THE PATIENT RECEIVED HIS NEW WHEELCHAIR RECENTLY, THE PATIENT'S WIFE THINKS THAT THE PINCH MIGHT HAVE BEEN CAUSED WHEN THE PATIENT WAS TRYING THE WHEELCHAIR, TO WHICH THE DOCTOR AGREED IT WAS POSSIBLE. SHE ASKED FOR A SEATING SPECIALIST TO INSPECT THE WHEELCHAIR BEFORE THE PATIENT START USING IT AGAIN.

  Patient problems: Abrasion

  MAUDE report 9825488 ↗