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Amysystems atrRecalls & reported problems

Amylior Inc · Alltrack power wheelchair series · Class 2

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

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00827482201738), received between Apr 5, 2021 and Apr 5, 2021 — classified as 1 death.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (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.

Most reported problems

Device problems

  • Insufficient Device Problem Information1

Patient problems

  • Crushing Injury1

Recent adverse event reports

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

  • DeathApr 5, 2021Insufficient Device Problem Information; Insufficient Device Problem Information

    MR. (B)(6) WAS VISITING THE BEACH; ONE THE CASTERS SHREDDED, HE SLAMMED INTO THE CURB AND THE CHAIR FLIPPED OVER HIM.

    Patient problems: Crushing Injury

    MAUDE report 11614593 ↗

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.