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MODULAR POWER POSITIONING SYSTEM 50T-RPSB- MAXXRecalls & reported problems

Motion Concepts Inc · DROP SEAT - MAXX RAIL · Class 2

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00754014710416), received between Jul 21, 2020 and Jul 21, 2020 — 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

Device problems

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryJul 21, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    ON (B)(6) 2020, MOTION CONCEPTS LP WAS NOTIFIED BY MEDBLOC INC. ((B)(4)), THAT ONE OF THEIR DEALER (NUMOTION) NOTIFIED THEM OF AN INCIDENT THAT TOOK PLACE ON (B)(6) 2020. THE DEALER REPORTED THAT THE END-USER WAS RIDING THE WHEELCHAIR AT THE PARKING LOT AND A VEHICLE HIT THE END-USER WHILE BACKING UP. THE DEALER ALSO MENTIONED THAT THERE WAS NO REPORTED INJURY TO THE END-USER AND THERE WAS NO DEVICE MALFUNCTION INVOLVED.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 10303841 ↗

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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.