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Permobil M400Recalls & reported problems

Permobil, Inc. · 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 17330818198768), received between Jun 22, 2022 and Jun 22, 2022 — 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

  • Bone Fracture(s)1
  • Limb Fracture1

Recent adverse event reports

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

  • InjuryJun 22, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    REPORT RECEIVED CLAIMING AS THE END-USER WAS DRIVING THEIR M400-HD OUTDOORS IN OFFROAD TERRAIN, THE WHEELCHAIR REPORTEDLY LOST UPRIGHT STABILITY AND ROLLED ONTO ITS SIDE, LANDED ATOP THE END-USER. REPORTS INDICATE THE END-USER RECEIVED INJURIES REQUIRING MEDICAL INTERVENTION TO ADDRESS.

    Patient problems: Bone Fracture(s); Limb Fracture

    MAUDE report 14774528 ↗

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.