MEDLINE WCAA0139Recalls & reported problems
Medline Industries, Inc. · ELEVATING LEGREST W/PAD,F/KR WC · Class 1
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00197344029917), received between Sep 23, 2026 and Sep 23, 2026 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Mechanical Jam” (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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Mechanical Jam2
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 23, 2026Mechanical Jam
It was reported that "one of the legrests she ordered is locked and she cannot get it to unlock."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50869253 ↗MalfunctionSep 23, 2026Mechanical Jam
It was reported that "the side broke".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50866965 ↗
Other COMPONENTS, WHEELCHAIR devices
- mo-Vis P002-77mo-Vis · Components, Wheelchair1 recall0 reports
- mo-Vis IDM-MICRO-Rmo-Vis · Components, Wheelchair1 recall0 reports
- mo-Vis P002-76mo-Vis · Components, Wheelchair1 recall0 reports
- mo-Vis P002-52mo-Vis · Components, Wheelchair1 recall0 reports
- mo-Vis P015-61mo-Vis · Components, Wheelchair1 recall0 reports
- mo-Vis P002-62mo-Vis · Components, Wheelchair1 recall0 reports
- munevo DRIVE V2Munevo Inc. · Components, Wheelchair1 recall0 reports
- mo-Vis IDM-MULTI-Rmo-Vis · Components, Wheelchair1 recall0 reports
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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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