Ki Little Wave FlipRecalls & reported problems
Ki Mobility, LLC · LITTLE WAVE FLIP 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 00850013379132), received between May 15, 2024 and May 15, 2024 — classified as 1 injury.
The most frequently reported specific device problem is “Use of Device Problem” (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.
Reports received per month
Most reported problems
Device problems
- Use of Device Problem1
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.
InjuryMay 15, 2024Use of Device Problem; Use of Device Problem
ACCORDING TO THE DEALER WHO REPORTED THE COMPLAINT; "THE INCIDENT WAS DUE TO CAREGIVER CARELESSNESS. THE INCIDENT OCCURRED DURING FULL ASSIST TRANSFER, PELVIC BELT WAS DOFF, AND CAREGIVER THOUGHT THE RELEASE CABLES ENGAGED THE WHEEL LOCK SYSTEM. THE CAREGIVER HAS TAKEN FULL RESPONSIBILITY."
Patient problems: Bone Fracture(s)
MAUDE report 19319667 ↗
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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