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Ki LibertyRecalls & reported problems

Ki Mobility, LLC · LIBERTY FT MANUAL WHEELCHAIR · Class 1

Data updated Oct 18, 2026 from official FDA records · Editorial policy

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 00850013379125), received between Dec 13, 2022 and Dec 13, 2022 — classified as 1 injury.

The most frequently reported specific device problem is “Missing 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Device problems

  • Missing Information1

Patient problems

  • Bone Fracture(s)1

Recent adverse event reports

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

  • InjuryDec 13, 2022Missing Information; Missing Information

    WHILE THE CHAIR WAS BEING TILTED, THE END USER'S FINGER WAS INJURED BY BEING PINCHED NEAR THE WHEEL LOCK. END USER'S HAND WAS IN THE AREA OF THE FRAME/WHEEL LOCK WHEN BEING TILTED. ALLEGED EVENT OCCURRED AT (B)(6) FACILITY DURING REHAB. AS PART OF THE INVESTIGATION, IT WAS DETERMINED THAT THE OWNER'S MANUAL INCLUDES WARNINGS OF THE PINCH POINTS IN QUESTION AND WAS PROVIDED TO THE END USERS' CAREGIVER AT DELIVERY OF THE WHEELCHAIR.

    Patient problems: Bone Fracture(s)

    MAUDE report 15970335 ↗

Other Wheelchair, mechanical devices

All Wheelchair, mechanical devices →

Sources and updates

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