MEDLINE KX228V21ERecalls & reported problems
Medline Industries, Inc. · WHEELCHAIR, XW, 22", RDLA, ELR · Class 1
- Adverse event reports
- 9
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 9 adverse event reports that list this exact device (DI 00193489179913), received between Apr 27, 2026 and Sep 30, 2026 — classified as 9 malfunctions.
The most frequently reported specific device problem is “Fracture” (4 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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Fracture4
- Material Twisted/Bent2
- Defective Device1
- Dent in Material1
- Loss of or Failure to Bond1
- Material Deformation1
- Mechanical Jam1
- Scratched Material1
Patient problems
- No Clinical Signs, Symptoms or Conditions9
Recent adverse event reports
The 9 most recent of 9 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 30, 2026Fracture
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50949944 ↗MalfunctionSep 30, 2026Fracture; Dent in Material; Scratched Material
It was reported that "Wheelchair received with a damaged wheel right out of the box.".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50945798 ↗MalfunctionSep 28, 2026Fracture; Material Twisted/Bent
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50920172 ↗MalfunctionSep 25, 2026Mechanical Jam
It was reported that the right side lever is stuck in up position and wont squeeze nor move.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50899209 ↗MalfunctionSep 24, 2026Fracture
It was reported that "Out of the box, one wheel of the 22" wheelchair frame was broken" and "The plastic wheel spokes that are attached to the frame are broken."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50882562 ↗MalfunctionSep 23, 2026Material Deformation
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50871106 ↗MalfunctionMay 14, 2026Material Twisted/Bent
IT WAS REPORTED UPON DELIVERY, THE WHEEL LOCKS ARE BENT OUTWARDS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25171531 ↗MalfunctionMay 8, 2026Loss of or Failure to Bond
PER CUSTOMER CALL, THE LEFT REAR WHEEL TREAD CAME OFF AND WILL NOT GO BACK ON.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25131388 ↗MalfunctionApr 27, 2026Defective Device
IT WAS REPORTED THAT THE FRONT WHEEL, WHEEL BEARING FELL OFF.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25009852 ↗
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
- Guardian K3186N24EMedline Industries, Inc. · Wheelchair, mechanical10 reports
- Quickie 7 SeriesSunrise Medical (US) LLC · Wheelchair, Mechanical1 death10 reports
- MEDLINE K3186N34SMedline Industries, Inc. · Wheelchair, mechanical9 reports
- Guardian K3206N24SMedline Industries, Inc. · Wheelchair, mechanical9 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.