MODULAR POWER STANDING SYSTEM MPSS-MINIRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00754014711451), received between Jul 5, 2022 and Jul 5, 2022 — classified as 1 injury.

The most frequently reported specific device problem is “Environmental Compatibility Problem” (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.

• InjuryJul 5, 2022Environmental Compatibility Problem; Insufficient Device Problem Information; Environmental Compatibility Problem; Insufficient Device Problem Information

  ON (B)(6) 2022, MOTION CONCEPTS LP WAS NOTIFIED BY (B)(6) THAT ONE OF THE DEALERS IN USA (B)(6) INFORMED THEM OF AN INCIDENT THAT WAS RELATED TO A MOTION CONCEPTS WHEELCHAIR. THEY NOTIFIED THAT THE END-USER WAS AT A SLANTED RAIL ON THE FISHING DOCK WHEN THE SYSTEM SUDDENLY STARTED TO TILT ON ITS OWN AND THE END-USER'S LEGS GOT PINNED UNDER THE RAIL. THEY ALSO REPORTED THAT HIS MOTHER WAS ABLE TO USE THE JOYSTICK TO GET THE SYSTEM AWAY FROM THE RAIL AND TO RETURN IT BACK TO ITS NORMAL POSITION. THE MOTHER MENTIONED TO THE DEALER THAT THE SYSTEM MALFUNCTIONED 3 MORE TIMES THROUGHOUT THE DAY AND THE SWITCHES DIDN'T GET PINNED UNDER THE RAILS, WHICH CAN CAUSE THE REPORTED ERROR. SHE ALSO STATED THAT THE END USER HAD JOYSTICKS AND BUTTONS PINNED ON PRIOR SYSTEMS THAT HE OWNED, WHICH IS WHY SHE PAYS CLOSE ATTENTION IN PREVENTING THAT. THE END-USER HAD SORE LEFT ANKLE AND BRUISING ON HIS SHINS DUE TO THIS INCIDENT.

  Patient problems: Bruise/Contusion; Pressure Sore/Ulcer

  MAUDE report 14914788 ↗