MODULAR POWER POSITIONING SYSTEM RS-12L-MAXXRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00754014711024), received between Nov 14, 2022 and Nov 14, 2022 — classified as 1 injury.

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.

• InjuryNov 14, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  ON (B)(6) 2022, MOTION CONCEPTS LP WAS NOTIFIED BY MEDBLOC INC., THAT ONE OF THE DEALERS IN USA (NUMOTION - OMAHA, NE) INFORMED THEM OF AN INCIDENT THAT WAS RELATED TO A MOTION CONCEPTS WHEELCHAIR. THEY NOTIFIED THAT THE END-USER WAS EXITING THE VAN BY GOING DOWN ON A RAMP IN HER WHEELCHAIR, WHEN THE WHEELCHAIR MOVED TO THE LEFT SIDE NEAR THE LIP OF THE RAMP. THE END-USER AND THE WHEELCHAIR FELL ON TO THE GARAGE CEMENT WHEN THE WHEELCHAIR WENT OVER THE LIP OF THE RAMP. THE DEALER ALSO REPORTED THAT THE END-USER MUST HAVE ACCIDENTLY HIT THE SPEED BUTTON, WHILE EXITING THE RAMP, WHICH MADE HER LOSE CONTROL OVER THE WHEELCHAIR. THE END-USER'S LEFT LEG HAD SCRAPED ELBOW, FRACTURED FEMUR AND TIBIA ON KNEE AND BROKEN PLATEAU. THEY ALSO REPORTED THAT THE END-USER HAD PAIN IN RIGHT SHIN AND BRUISE IN RIGHT FOOT AND ANKLE DUE TO THIS INCIDENT.

  Patient problems: Bone Fracture(s); Bruise/Contusion

  MAUDE report 15789175 ↗