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Amysystems athdRecalls & reported problems

Amylior Inc · Alltrack power wheelchair series · Class 2

Adverse event reports
3
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00827482201721), received between Jan 13, 2026 and Jun 30, 2026 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Device Slipped” (2 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: 1 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 1 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 Slipped2
  • Device Tipped Over1

Patient problems

  • Abrasion1
  • Concussion1
  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJun 30, 2026Device Slipped

    THE WHEELCHAIR OVERTURNED TWICE WITH THE USER INSIDE. THE FIRST TIME (B)(6) 2026, THE USER WAS PULLING INTO THE DRIVEWAY WHEN THE FRONT WHEELS SLIPPED AND THE WHEELCHAIR BEGAN TO TIP OVER COMPLETELY; THE USER FELL ON HER RIGHT SIDE, HITTING HER HEAD AND ELBOW, WHILE HER KNEES WERE SCRATCHED AND BLEEDING. THE SECOND TIME (B)(6) 2026, WHILE THE USER WAS SEATED IN HER WHEELCHAIR, THE DRIVER MADE A TURN; THE WHEELCHAIR SKIDDED TO THE LEFT AND TIPPED OVER, THROWING HER AGAINST THE LEFT DOOR OF THE VAN WHERE SHE BECAME TRAPPED ON HER SIDE, HITTING HER HEAD AND ELBOW. EMERGENCY SERVICES (911) WERE CALLED IN BOTH CASES. SHE WAS WEARING HER SEATBELT.

    Patient problems: Abrasion

    MAUDE report 25664234 ↗
  • MalfunctionMar 2, 2026Device Tipped Over

    USER IN HIS WHEELCHAIR WAS INVOLVED IN AN ACCIDENT, BUT WE DO NOT HAVE DETAILS OF HOW OR WHEN HE FELL OUT OF THE CHAIR. HE LEANS HEAVILY TO THE LEFT SIDE, DRIVES THE CHAIR UP AND DOWN THE STREET, AND THE STORY WE GOT WAS HE WAS TRAVERSING A SIDEWALK AND TRIED TO GO OVER A CURB THAT WAS TOO HIGH. HE WAS NOT HOSPITALIZED AND THERE ARE NO BRUISES.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 24483847 ↗
  • MalfunctionJan 13, 2026Device Slipped

    THE USER FLIPPED OUT OF HIS CHAIR (B)(6) 2025. HE WAS GOING UP HIS RAMP ON HIS WHEELCHAIR-ACCESSIBLE VAN AND THE CHAIR STARTED SLIDING BACKWARDS, EVENTUALLY TIPPING OVER; THIS CAUSED HIM TO HIT HIS HEAD ON THE CONCRETE. HE WENT TO THE ER FOR TESTS, WAS RELEASED TO GO HOME AND AFTER A FEW DAYS, NEEDED TO GO BACK TO THE ER, TO BE DIAGNOSED WITH A CONCUSSION.

    Patient problems: Concussion

    MAUDE report 24054819 ↗

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.