MEDLINE INDUSTRIES, INC. MDS806560Recalls & reported problems
Medline Industries, Inc. · WHEELCHAIR,K4 LIGHT,20",DLA,S/A FOOT · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10080196739592), received between Apr 23, 2024 and Sep 29, 2026 — classified as 1 injury, 3 malfunctions.
The most frequently reported specific device problem is “Activation 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
- Activation Problem1
- Appropriate Device Problem Term/Code Not Available1
- Fracture1
- Material Twisted/Bent1
- Mechanical Jam1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
- Abdominal Pain1
- Bone Fracture(s)1
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 29, 2026Fracture; Mechanical Jam
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50932637 ↗MalfunctionSep 26, 2026Activation Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50909443 ↗MalfunctionJun 17, 2026Material Twisted/Bent
IT WAS REPORTED THAT "THE BOTH SIDE SEAT RAILS ARE BENT INWARDS PREVENTING HIM FROM CLOSING THE WHEELCHAIR".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25539677 ↗InjuryApr 23, 2024Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
ACCORDING TO THE CUSTOMER ON (B)(6) 2024 "THEY WERE LEAVING THE OFFICE BUILDING THAT THEIR DOCTOR IS IN AND GOING TO THEIR CAR WHEN THE BOLT THAT HOLDS THE FRONT WHEEL IN PLACE SNAPPED AND SENT ME FALLING TO THE ASPHALT".
Patient problems: Abdominal Pain; Bone Fracture(s)
MAUDE report 19166538 ↗
Other Wheelchair, mechanical devices
- MEDLINE K1186N22SMedline Industries, Inc. · Wheelchair, mechanical48 reports
- Guardian K4186N24EMedline Industries, Inc. · Wheelchair, mechanical22 reports
- MEDLINE INDUSTRIES, INC. MDS808650Medline Industries, Inc. · Wheelchair, mechanical18 reports
- Medline MDS806850Medline Industries, Inc. · Wheelchair, mechanical17 reports
- Quickie 7 SeriesSunrise Medical (US) LLC · Wheelchair, Mechanical1 death10 reports
- Guardian K3186N24EMedline Industries, Inc. · Wheelchair, mechanical10 reports
- Guardian K3206N24SMedline Industries, Inc. · Wheelchair, mechanical9 reports
- MEDLINE K3186N34SMedline Industries, Inc. · Wheelchair, mechanical9 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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