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Amysystems atmRecalls & reported problems

Amylior Inc · Alltrack powerchairs series · Class 2

Adverse event reports
4
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00827482201714), received between Jun 2, 2021 and Jan 13, 2026 — classified as 1 injury, 3 malfunctions.

The most frequently reported specific device problem is “Device Tipped Over” (3 reports).

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: 0 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: 1 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 Tipped Over3
  • Unintended Ejection1

Patient problems

  • No Clinical Signs, Symptoms or Conditions2
  • Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
  • Insufficient Information1

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJan 13, 2026Device Tipped Over

    THE END USER HIT SOMETHING OR THE RIGHT MOTOR JUST STOPPED WORKING, THE CHAIR PULLED TO THE RIGHT (JUST THE LEFT HAND SIDE MOTOR WORKING) AND FELL OFF OF THE CURB EJECTING THE USER OUT OF THE CHAIR. NO INJURIES, NO HOSPITALISATION. ONLY DAMAGE AFTER INSPECTION WAS A BENT R/H FORK.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 24055140 ↗
  • MalfunctionNov 9, 2022Unintended Ejection; Unintended Ejection

    WHILE DRIVING HIS MOTORIZED WHEELCHAIR ON A STRIP OF PAVEMENT, THE BENEFICIARY ENDED UP ON HIS SIDE, DAMAGING PART OF THE WHEELCHAIR. NO OTHER INFO AVAILABLE (INJURY, HOSPITALIZATION, ETC).

    Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available

    MAUDE report 15762595 ↗
  • MalfunctionNov 9, 2022Device Tipped Over; Device Tipped Over

    THE END USER TIPPED FORWARD WHILE DRIVING THE CHAIR DOWN ON A HILL. APPARENTLY, AT THE END OF THE HILL THERE WAS A POTHOLE FILLED WITH WATER AND THE FRONT CASTERS FELL INTO THE POTHOLE TIPPING THE CHAIR OVER. THE END USER GOT A FOOT STUCK UNDER THE FOOT PEDAL (SEAT BELTED IN): WAS HOSPITALIZED FOR A DAY BUT NO PHYSICAL DAMAGE TO FOOT, NO SORES, NOTHING BROKEN (X-RAYS TAKEN). THE MOTORS AND THE JOYSTICK WERE IN THE WATER ; MOTORS ARE STILL WORKING FINE 3 WEEKS AFTER THE ACCIDENT BUT JOYSTICK WAS DAMAGED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 15761772 ↗
  • InjuryJun 2, 2021Device Tipped Over; Device Tipped Over

    MR (B)(6) REPORTS TILTING HIS CHAIR IN HIS BEDROOM ON A FLAT SURFACE AND THE CHAIR TIPPED BACKWARD WITH HIM STILL IN IT. HE WAS NOT EJECTED FROM THE CHAIR BUT WAS HOSPITALIZED FOR APPROXIMATELY A WEEK AND RELEASED.

    Patient problems: Insufficient Information

    MAUDE report 11922127 ↗

Other Wheelchair, Powered devices

All Wheelchair, Powered devices →

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