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MODULAR POWER POSITIONING SYSTEM 45T-12L-MAXXRecalls & reported problems

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

Adverse event reports
2
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00754014710034), received between Jun 21, 2022 and Nov 14, 2024 — classified as 1 injury, 1 malfunction.

The most frequently reported specific device problem is “Device Handling 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.

Reports received per month

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 1 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520261
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Device Handling Problem1
  • Misassembly During Maintenance/Repair1
  • Self-Activation or Keying1

Patient problems

  • Bruise/Contusion1
  • Multiple Fractures1

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • MalfunctionNov 14, 2024Self-Activation or Keying; Self-Activation or Keying

    ON OCTOBER 15, 2024, MEDBLOC (DISTRIBUTOR) NOTIFIED MOTION CONCEPTS LP OF AN INCIDENT INVOLVING ONE OF OUR WHEELCHAIRS. THE PRODUCT HAD BEEN SOLD TO THE END-USER IN THE USA BY A DEALER, AMERICAN SEATING & MOBILITY IN (B)(6), WHO WAS ALSO RESPONSIBLE FOR ITS MAINTENANCE. THE DEALER HAD INSTALLED A THIRD-PARTY HEAD ARRAY ON THE WHEELCHAIR. ACCORDING TO THE END-USER, WHILE USING THE WHEELCHAIR IN AN OFFICE ROOM, THE HEAD ARRAY UNEXPECTEDLY ACTIVATED, CAUSING THE WHEELCHAIR TO ACCELERATE TOWARD A DESK. AS A RESULT, THE END-USER SUSTAINED BRUISING AND SCRATCHES ON THE LEFT LEG BUT DID NOT REQUIRE MEDICAL ASSISTANCE. THE SYSTEM HAD BEEN IN USE FOR APPROXIMATELY FOUR MONTHS AT THE TIME OF THE INCIDENT.

    Patient problems: Bruise/Contusion

    MAUDE report 20689312 ↗
  • InjuryJun 21, 2022Device Handling Problem; Misassembly During Maintenance/Repair; Device Handling Problem; Misassembly During Maintenance/Repair

    ON 26-MAY-2022, MOTION CONCEPTS LP WAS NOTIFIED BY (B)(4), THAT ONE OF THE DEALERS IN USA ((B)(4)) INFORMED THEM OF AN INCIDENT THAT WAS RELATED TO A MOTION CONCEPTS WHEELCHAIR. THE WHEELCHAIR WAS SOLD TO (B)(4) BUT, (B)(4) WAS MAINTAINING IT. THEY NOTIFIED THAT THE END-USER WAS DRIVING HIS WHEELCHAIR WHEN HE SUDDENLY FELL FORWARD AND WHEELCHAIR FELL ON TOP OF THE END-USER. THE END-USER FRACTURED BOTH HIS ANKLES AND HAD TO WEAR CAST FROM KNEE DOWN. THE DEALER CONFIRMED THAT THEY HAD ADJUSTED THE SEAT DEPTH FORWARD BY 2" ON 13-MAY-2022 AND THE END-USER WAS NOT WEARING SEAT BELT OR CHEST STRAP AS THE BUCKLE ON THE SEAT BELT WAS DAMAGED BEFORE THE INCIDENT.

    Patient problems: Multiple Fractures

    MAUDE report 14755855 ↗

Other Wheelchair, Powered devices

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